Name: rs67757094
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs67757094

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:186932295-186932307 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₆ / delTT / delT / dupT / du…
del(T)₆ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / ins(T)₁₄ / ins(T)₁₇ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.000023 (6/264690, TOPMED)
delT=0.2116 (1737/8208, ALFA)
delT=0.3592 (1799/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PLA2G4A : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	8208	TTTTTTTTTTTTT=0.7131	TTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.2116, TTTTTTTTTTTTTT=0.0658, TTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTT=0.0023, TTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTT=0.0000	0.66075	0.072415	0.266836	32
European	Sub	7340	TTTTTTTTTTTTT=0.6796	TTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.2364, TTTTTTTTTTTTTT=0.0734, TTTTTTTTTTTTTTTT=0.0030, TTTTTTTTTTTTTTTTTTTT=0.0026, TTTTTTTTTTTTTTTTT=0.0023, TTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTT=0.0000	0.614249	0.082478	0.303273	32
African	Sub	534	TTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	TTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	518	TTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	TTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	TTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	16	TTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	196	TTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	20	TTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	92	TTTTTTTTTTTTT=0.97	TTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.02, TTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	0.955556	0.0	0.044444	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₁₃=0.999977	del(T)₆=0.000023
Allele Frequency Aggregator	Total	Global	8208	(T)₁₃=0.7131	del(T)₆=0.0000, delTT=0.0000, delT=0.2116, dupT=0.0658, dupTT=0.0000, dupTTT=0.0027, dup(T)₄=0.0021, dup(T)₆=0.0024, dup(T)₇=0.0023
Allele Frequency Aggregator	European	Sub	7340	(T)₁₃=0.6796	del(T)₆=0.0000, delTT=0.0000, delT=0.2364, dupT=0.0734, dupTT=0.0000, dupTTT=0.0030, dup(T)₄=0.0023, dup(T)₆=0.0027, dup(T)₇=0.0026
Allele Frequency Aggregator	African	Sub	534	(T)₁₃=1.000	del(T)₆=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	196	(T)₁₃=1.000	del(T)₆=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	92	(T)₁₃=0.97	del(T)₆=0.00, delTT=0.00, delT=0.02, dupT=0.01, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(T)₁₃=1.00	del(T)₆=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(T)₁₃=1.00	del(T)₆=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	10	(T)₁₃=1.0	del(T)₆=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0, dup(T)₇=0.0
1000Genomes	Global	Study-wide	5008	(T)₁₃=0.6408	delT=0.3592
1000Genomes	African	Sub	1322	(T)₁₃=0.9266	delT=0.0734
1000Genomes	East Asian	Sub	1008	(T)₁₃=0.4762	delT=0.5238
1000Genomes	Europe	Sub	1006	(T)₁₃=0.4175	delT=0.5825
1000Genomes	South Asian	Sub	978	(T)₁₃=0.633	delT=0.367
1000Genomes	American	Sub	694	(T)₁₃=0.670	delT=0.330

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.186932302_186932307del
GRCh38.p14 chr 1	NC_000001.11:g.186932306_186932307del
GRCh38.p14 chr 1	NC_000001.11:g.186932307del
GRCh38.p14 chr 1	NC_000001.11:g.186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932306_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932305_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932304_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932303_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932302_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932301_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932300_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932299_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932298_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932297_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932296_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932295_186932307dup
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901434_186901439del
GRCh37.p13 chr 1	NC_000001.10:g.186901438_186901439del
GRCh37.p13 chr 1	NC_000001.10:g.186901439del
GRCh37.p13 chr 1	NC_000001.10:g.186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901438_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901437_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901436_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901435_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901434_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901433_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901432_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901431_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901430_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901429_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901428_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901427_186901439dup
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108403_108408del
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108407_108408del
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408del
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108407_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108406_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108405_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108404_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108403_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108402_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108401_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108400_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108399_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108398_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108397_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108396_108408dup
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTTT

Gene: PLA2G4A, phospholipase A2 group IVA (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PLA2G4A transcript variant 2	NM_001311193.2:c.379-461_… NM_001311193.2:c.379-461_379-456del	N/A	Intron Variant
PLA2G4A transcript variant 1	NM_024420.3:c.559-461_559… NM_024420.3:c.559-461_559-456del	N/A	Intron Variant
PLA2G4A transcript variant X1	XM_005245267.5:c.574-461_… XM_005245267.5:c.574-461_574-456del	N/A	Intron Variant
PLA2G4A transcript variant X2	XM_011509642.3:c.559-461_… XM_011509642.3:c.559-461_559-456del	N/A	Intron Variant
PLA2G4A transcript variant X3	XM_047422599.1:c.559-461_… XM_047422599.1:c.559-461_559-456del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₃=	del(T)₆	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	ins(T)₁₄	ins(T)₁₇	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃
GRCh38.p14 chr 1	NC_000001.11:g.186932295_186932307=	NC_000001.11:g.186932302_186932307del	NC_000001.11:g.186932306_186932307del	NC_000001.11:g.186932307del	NC_000001.11:g.186932307dup	NC_000001.11:g.186932306_186932307dup	NC_000001.11:g.186932305_186932307dup	NC_000001.11:g.186932304_186932307dup	NC_000001.11:g.186932303_186932307dup	NC_000001.11:g.186932302_186932307dup	NC_000001.11:g.186932301_186932307dup	NC_000001.11:g.186932300_186932307dup	NC_000001.11:g.186932299_186932307dup	NC_000001.11:g.186932298_186932307dup	NC_000001.11:g.186932297_186932307dup	NC_000001.11:g.186932296_186932307dup	NC_000001.11:g.186932295_186932307dup	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTT	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTT	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.186901427_186901439=	NC_000001.10:g.186901434_186901439del	NC_000001.10:g.186901438_186901439del	NC_000001.10:g.186901439del	NC_000001.10:g.186901439dup	NC_000001.10:g.186901438_186901439dup	NC_000001.10:g.186901437_186901439dup	NC_000001.10:g.186901436_186901439dup	NC_000001.10:g.186901435_186901439dup	NC_000001.10:g.186901434_186901439dup	NC_000001.10:g.186901433_186901439dup	NC_000001.10:g.186901432_186901439dup	NC_000001.10:g.186901431_186901439dup	NC_000001.10:g.186901430_186901439dup	NC_000001.10:g.186901429_186901439dup	NC_000001.10:g.186901428_186901439dup	NC_000001.10:g.186901427_186901439dup	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTT	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTT	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A RefSeqGene (LRG_596)	NG_012203.2:g.108396_108408=	NG_012203.2:g.108403_108408del	NG_012203.2:g.108407_108408del	NG_012203.2:g.108408del	NG_012203.2:g.108408dup	NG_012203.2:g.108407_108408dup	NG_012203.2:g.108406_108408dup	NG_012203.2:g.108405_108408dup	NG_012203.2:g.108404_108408dup	NG_012203.2:g.108403_108408dup	NG_012203.2:g.108402_108408dup	NG_012203.2:g.108401_108408dup	NG_012203.2:g.108400_108408dup	NG_012203.2:g.108399_108408dup	NG_012203.2:g.108398_108408dup	NG_012203.2:g.108397_108408dup	NG_012203.2:g.108396_108408dup	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTT	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTT	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTT	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTT	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTT	NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant 2	NM_001311193.2:c.379-468=	NM_001311193.2:c.379-461_379-456del	NM_001311193.2:c.379-457_379-456del	NM_001311193.2:c.379-456del	NM_001311193.2:c.379-456dup	NM_001311193.2:c.379-457_379-456dup	NM_001311193.2:c.379-458_379-456dup	NM_001311193.2:c.379-459_379-456dup	NM_001311193.2:c.379-460_379-456dup	NM_001311193.2:c.379-461_379-456dup	NM_001311193.2:c.379-462_379-456dup	NM_001311193.2:c.379-463_379-456dup	NM_001311193.2:c.379-464_379-456dup	NM_001311193.2:c.379-465_379-456dup	NM_001311193.2:c.379-466_379-456dup	NM_001311193.2:c.379-467_379-456dup	NM_001311193.2:c.379-468_379-456dup	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTT	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTTTTT	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTT	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTT	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTTT	NM_001311193.2:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant 1	NM_024420.2:c.559-468=	NM_024420.2:c.559-461_559-456del	NM_024420.2:c.559-457_559-456del	NM_024420.2:c.559-456del	NM_024420.2:c.559-456dup	NM_024420.2:c.559-457_559-456dup	NM_024420.2:c.559-458_559-456dup	NM_024420.2:c.559-459_559-456dup	NM_024420.2:c.559-460_559-456dup	NM_024420.2:c.559-461_559-456dup	NM_024420.2:c.559-462_559-456dup	NM_024420.2:c.559-463_559-456dup	NM_024420.2:c.559-464_559-456dup	NM_024420.2:c.559-465_559-456dup	NM_024420.2:c.559-466_559-456dup	NM_024420.2:c.559-467_559-456dup	NM_024420.2:c.559-468_559-456dup	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTT	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTTTTT	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTT	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTT	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTT	NM_024420.2:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant 1	NM_024420.3:c.559-468=	NM_024420.3:c.559-461_559-456del	NM_024420.3:c.559-457_559-456del	NM_024420.3:c.559-456del	NM_024420.3:c.559-456dup	NM_024420.3:c.559-457_559-456dup	NM_024420.3:c.559-458_559-456dup	NM_024420.3:c.559-459_559-456dup	NM_024420.3:c.559-460_559-456dup	NM_024420.3:c.559-461_559-456dup	NM_024420.3:c.559-462_559-456dup	NM_024420.3:c.559-463_559-456dup	NM_024420.3:c.559-464_559-456dup	NM_024420.3:c.559-465_559-456dup	NM_024420.3:c.559-466_559-456dup	NM_024420.3:c.559-467_559-456dup	NM_024420.3:c.559-468_559-456dup	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTT	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTTTTT	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTT	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTT	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTT	NM_024420.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant X1	XM_005245267.1:c.448-468=	XM_005245267.1:c.448-461_448-456del	XM_005245267.1:c.448-457_448-456del	XM_005245267.1:c.448-456del	XM_005245267.1:c.448-456dup	XM_005245267.1:c.448-457_448-456dup	XM_005245267.1:c.448-458_448-456dup	XM_005245267.1:c.448-459_448-456dup	XM_005245267.1:c.448-460_448-456dup	XM_005245267.1:c.448-461_448-456dup	XM_005245267.1:c.448-462_448-456dup	XM_005245267.1:c.448-463_448-456dup	XM_005245267.1:c.448-464_448-456dup	XM_005245267.1:c.448-465_448-456dup	XM_005245267.1:c.448-466_448-456dup	XM_005245267.1:c.448-467_448-456dup	XM_005245267.1:c.448-468_448-456dup	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTT	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTTTTT	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTTTTTTTT	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTTTTTTTTT	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTTTTTTTTTT	XM_005245267.1:c.448-456_448-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant X1	XM_005245267.5:c.574-468=	XM_005245267.5:c.574-461_574-456del	XM_005245267.5:c.574-457_574-456del	XM_005245267.5:c.574-456del	XM_005245267.5:c.574-456dup	XM_005245267.5:c.574-457_574-456dup	XM_005245267.5:c.574-458_574-456dup	XM_005245267.5:c.574-459_574-456dup	XM_005245267.5:c.574-460_574-456dup	XM_005245267.5:c.574-461_574-456dup	XM_005245267.5:c.574-462_574-456dup	XM_005245267.5:c.574-463_574-456dup	XM_005245267.5:c.574-464_574-456dup	XM_005245267.5:c.574-465_574-456dup	XM_005245267.5:c.574-466_574-456dup	XM_005245267.5:c.574-467_574-456dup	XM_005245267.5:c.574-468_574-456dup	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTT	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTTTTT	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTTTTTTTT	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTTTTTTTTT	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTTTTTTTTTT	XM_005245267.5:c.574-456_574-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant X2	XM_005245268.1:c.379-468=	XM_005245268.1:c.379-461_379-456del	XM_005245268.1:c.379-457_379-456del	XM_005245268.1:c.379-456del	XM_005245268.1:c.379-456dup	XM_005245268.1:c.379-457_379-456dup	XM_005245268.1:c.379-458_379-456dup	XM_005245268.1:c.379-459_379-456dup	XM_005245268.1:c.379-460_379-456dup	XM_005245268.1:c.379-461_379-456dup	XM_005245268.1:c.379-462_379-456dup	XM_005245268.1:c.379-463_379-456dup	XM_005245268.1:c.379-464_379-456dup	XM_005245268.1:c.379-465_379-456dup	XM_005245268.1:c.379-466_379-456dup	XM_005245268.1:c.379-467_379-456dup	XM_005245268.1:c.379-468_379-456dup	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTT	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTTTTT	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTT	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTT	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTTT	XM_005245268.1:c.379-456_379-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant X2	XM_011509642.3:c.559-468=	XM_011509642.3:c.559-461_559-456del	XM_011509642.3:c.559-457_559-456del	XM_011509642.3:c.559-456del	XM_011509642.3:c.559-456dup	XM_011509642.3:c.559-457_559-456dup	XM_011509642.3:c.559-458_559-456dup	XM_011509642.3:c.559-459_559-456dup	XM_011509642.3:c.559-460_559-456dup	XM_011509642.3:c.559-461_559-456dup	XM_011509642.3:c.559-462_559-456dup	XM_011509642.3:c.559-463_559-456dup	XM_011509642.3:c.559-464_559-456dup	XM_011509642.3:c.559-465_559-456dup	XM_011509642.3:c.559-466_559-456dup	XM_011509642.3:c.559-467_559-456dup	XM_011509642.3:c.559-468_559-456dup	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTT	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTTTTT	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTT	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTT	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTT	XM_011509642.3:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTTT
PLA2G4A transcript variant X3	XM_047422599.1:c.559-468=	XM_047422599.1:c.559-461_559-456del	XM_047422599.1:c.559-457_559-456del	XM_047422599.1:c.559-456del	XM_047422599.1:c.559-456dup	XM_047422599.1:c.559-457_559-456dup	XM_047422599.1:c.559-458_559-456dup	XM_047422599.1:c.559-459_559-456dup	XM_047422599.1:c.559-460_559-456dup	XM_047422599.1:c.559-461_559-456dup	XM_047422599.1:c.559-462_559-456dup	XM_047422599.1:c.559-463_559-456dup	XM_047422599.1:c.559-464_559-456dup	XM_047422599.1:c.559-465_559-456dup	XM_047422599.1:c.559-466_559-456dup	XM_047422599.1:c.559-467_559-456dup	XM_047422599.1:c.559-468_559-456dup	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTT	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTTTTT	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTT	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTT	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTT	XM_047422599.1:c.559-456_559-455insTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

72 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95249082	Oct 11, 2018 (152)
2	HUMANGENOME_JCVI	ss95951495	Mar 15, 2016 (147)
3	GMI	ss287684571	May 09, 2011 (137)
4	GMI	ss288066267	Jan 10, 2018 (151)
5	GMI	ss288066269	May 04, 2012 (137)
6	GMI	ss288066271	Oct 11, 2018 (152)
7	PJP	ss294615171	May 09, 2011 (137)
8	PJP	ss294615172	Oct 11, 2018 (152)
9	SSMP	ss663140005	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666119351	Apr 25, 2013 (138)
11	1000GENOMES	ss1367926520	Aug 21, 2014 (142)
12	EVA_UK10K_TWINSUK	ss1701530816	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1701530823	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1709961281	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1709961287	Apr 01, 2015 (144)
16	SWEGEN	ss2988110001	Nov 08, 2017 (151)
17	EVA_DECODE	ss3688214789	Jul 12, 2019 (153)
18	EVA_DECODE	ss3688214790	Jul 12, 2019 (153)
19	EVA_DECODE	ss3688214791	Jul 12, 2019 (153)
20	ACPOP	ss3727676839	Jul 12, 2019 (153)
21	ACPOP	ss3727676840	Jul 12, 2019 (153)
22	PACBIO	ss3783629335	Jul 12, 2019 (153)
23	PACBIO	ss3789250294	Jul 12, 2019 (153)
24	PACBIO	ss3794122432	Jul 12, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3800081239	Jul 12, 2019 (153)
26	EVA	ss3826537927	Apr 25, 2020 (154)
27	EVA	ss3836665472	Apr 25, 2020 (154)
28	EVA	ss3842075917	Apr 25, 2020 (154)
29	GNOMAD	ss4007589104	Apr 25, 2021 (155)
30	GNOMAD	ss4007589105	Apr 25, 2021 (155)
31	GNOMAD	ss4007589106	Apr 25, 2021 (155)
32	GNOMAD	ss4007589107	Apr 25, 2021 (155)
33	GNOMAD	ss4007589108	Apr 25, 2021 (155)
34	GNOMAD	ss4007589109	Apr 25, 2021 (155)
35	GNOMAD	ss4007589110	Apr 25, 2021 (155)
36	GNOMAD	ss4007589111	Apr 25, 2021 (155)
37	GNOMAD	ss4007589112	Apr 25, 2021 (155)
38	GNOMAD	ss4007589113	Apr 25, 2021 (155)
39	GNOMAD	ss4007589114	Apr 25, 2021 (155)
40	GNOMAD	ss4007589115	Apr 25, 2021 (155)
41	GNOMAD	ss4007589116	Apr 25, 2021 (155)
42	GNOMAD	ss4007589117	Apr 25, 2021 (155)
43	GNOMAD	ss4007589118	Apr 25, 2021 (155)
44	GNOMAD	ss4007589119	Apr 25, 2021 (155)
45	GNOMAD	ss4007589120	Apr 25, 2021 (155)
46	GNOMAD	ss4007589121	Apr 25, 2021 (155)
47	GNOMAD	ss4007589122	Apr 25, 2021 (155)
48	GNOMAD	ss4007589124	Apr 25, 2021 (155)
49	GNOMAD	ss4007589125	Apr 25, 2021 (155)
50	TOPMED	ss4476184071	Apr 25, 2021 (155)
51	TOMMO_GENOMICS	ss5147486569	Apr 25, 2021 (155)
52	TOMMO_GENOMICS	ss5147486570	Apr 25, 2021 (155)
53	TOMMO_GENOMICS	ss5147486571	Apr 25, 2021 (155)
54	TOMMO_GENOMICS	ss5147486572	Apr 25, 2021 (155)
55	TOMMO_GENOMICS	ss5147486573	Apr 25, 2021 (155)
56	TOMMO_GENOMICS	ss5147486574	Apr 25, 2021 (155)
57	1000G_HIGH_COVERAGE	ss5245065273	Oct 12, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5245065274	Oct 12, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5245065275	Oct 12, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5245065276	Oct 12, 2022 (156)
61	HUGCELL_USP	ss5445572786	Oct 12, 2022 (156)
62	HUGCELL_USP	ss5445572787	Oct 12, 2022 (156)
63	HUGCELL_USP	ss5445572788	Oct 12, 2022 (156)
64	HUGCELL_USP	ss5445572789	Oct 12, 2022 (156)
65	TOMMO_GENOMICS	ss5674975048	Oct 12, 2022 (156)
66	TOMMO_GENOMICS	ss5674975049	Oct 12, 2022 (156)
67	TOMMO_GENOMICS	ss5674975050	Oct 12, 2022 (156)
68	TOMMO_GENOMICS	ss5674975051	Oct 12, 2022 (156)
69	TOMMO_GENOMICS	ss5674975052	Oct 12, 2022 (156)
70	TOMMO_GENOMICS	ss5674975053	Oct 12, 2022 (156)
71	EVA	ss5832970465	Oct 12, 2022 (156)
72	EVA	ss5832970466	Oct 12, 2022 (156)
73	1000Genomes	NC_000001.10 - 186901427	Oct 11, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2546506 (NC_000001.10:186901426:T: 1897/3854) Row 2546507 (NC_000001.10:186901426::T 632/3854)	-	Oct 11, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2546506 (NC_000001.10:186901426:T: 1897/3854) Row 2546507 (NC_000001.10:186901426::T 632/3854)	-	Oct 11, 2018 (152)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33487104 (NC_000001.11:186932294::T 36948/127200) Row 33487105 (NC_000001.11:186932294::TT 168/127248) Row 33487106 (NC_000001.11:186932294::TTT 13/127288)...	-	Apr 25, 2021 (155)
97	Northern Sweden Submission ignored due to conflicting rows: Row 961704 (NC_000001.10:186901426:T: 278/596) Row 961705 (NC_000001.10:186901426::T 65/596)	-	Jul 12, 2019 (153)
98	Northern Sweden Submission ignored due to conflicting rows: Row 961704 (NC_000001.10:186901426:T: 278/596) Row 961705 (NC_000001.10:186901426::T 65/596)	-	Jul 12, 2019 (153)
99	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 5455876 (NC_000001.10:186901426:T: 7589/16756) Row 5455877 (NC_000001.10:186901426::T 6192/16756) Row 5455878 (NC_000001.10:186901426:TT: 78/16756)...	-	Apr 25, 2021 (155)
105	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 8812152 (NC_000001.11:186932294::T 9954/28130) Row 8812153 (NC_000001.11:186932294:T: 12824/28130) Row 8812154 (NC_000001.11:186932294:TT: 140/28130)...	-	Oct 12, 2022 (156)
111	TopMed	NC_000001.11 - 186932295	Apr 25, 2021 (155)
112	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2546506 (NC_000001.10:186901426:T: 1858/3708) Row 2546507 (NC_000001.10:186901426::T 614/3708)	-	Oct 11, 2018 (152)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2546506 (NC_000001.10:186901426:T: 1858/3708) Row 2546507 (NC_000001.10:186901426::T 614/3708)	-	Oct 11, 2018 (152)
114	ALFA	NC_000001.11 - 186932295	Apr 25, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs67906241	May 11, 2012 (137)
rs67906242	Feb 27, 2009 (130)
rs374651872	May 13, 2013 (138)
rs796583468	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5147486574	NC_000001.10:186901426:TTTTTT:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTT	(self)
39790406, ss4476184071, ss5674975053	NC_000001.11:186932294:TTTTTT:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTT	(self)
ss288066267	NC_000001.9:185168049:TT:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5147486571	NC_000001.10:186901426:TT:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4007589125, ss5245065276, ss5445572786, ss5674975050	NC_000001.11:186932294:TT:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288066269, ss294615171	NC_000001.9:185168049:T:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4641519, ss663140005, ss666119351, ss1367926520, ss1701530816, ss1701530823, ss2988110001, ss3727676839, ss3836665472, ss5147486569, ss5832970465	NC_000001.10:186901426:T:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3688214789, ss3800081239, ss3842075917, ss4007589124, ss5245065274, ss5445572787, ss5674975049	NC_000001.11:186932294:T:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss287684571	NT_004487.19:38390068:T:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss95951495	NT_004487.19:38390080:T:	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss294615172	NC_000001.9:185168056::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss288066271	NC_000001.9:185168062::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3727676840, ss3783629335, ss3789250294, ss3794122432, ss3826537927, ss5147486570, ss5832970466	NC_000001.10:186901426::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1709961281, ss1709961287	NC_000001.10:186901427::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4007589104, ss5245065273, ss5445572788, ss5674975048	NC_000001.11:186932294::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3688214790	NC_000001.11:186932295::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss95951495	NT_004487.19:38390080:T:TT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss95249082	NT_004487.19:38390081::T	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5147486573	NC_000001.10:186901426::TT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4007589105, ss5245065275, ss5445572789, ss5674975052	NC_000001.11:186932294::TT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4007589106	NC_000001.11:186932294::TTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4007589107	NC_000001.11:186932294::TTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4007589108	NC_000001.11:186932294::TTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4007589109	NC_000001.11:186932294::TTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5147486572	NC_000001.10:186901426::TTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4007589110, ss5674975051	NC_000001.11:186932294::TTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
587224593	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4007589111	NC_000001.11:186932294::TTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589112	NC_000001.11:186932294::TTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589113	NC_000001.11:186932294::TTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3688214791	NC_000001.11:186932295::TTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589114	NC_000001.11:186932294::TTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589115	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589116	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589117	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589118	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589119	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589120	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589121	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007589122	NC_000001.11:186932294::TTTTTTTTTT… NC_000001.11:186932294::TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:186932294:TTTTTTTTTTT… NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs67757094

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs67757094