Name: rs67863152
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.

rs67863152

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:78470883-78470902 (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)₈ / del(T)₇ / del(T)₅ / del(…
del(T)₈ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / 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)₁₁ / dup(T)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1909 (848/4442, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NARS2 : Intron Variant
LOC105369403 : Non Coding Transcript 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	4442	TTTTTTTTTTTTTTTTTTTT=0.1297	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.1909, TTTTTTTTTTTTTTTTTTTTTT=0.5867, TTTTTTTTTTTTTTTTTTTTTTT=0.0835, TTTTTTTTTTTTTTTTTTTTTTTT=0.0036, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0036, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.108886	0.616395	0.274718	32
European	Sub	4424	TTTTTTTTTTTTTTTTTTTT=0.1279	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.1912, TTTTTTTTTTTTTTTTTTTTTT=0.5877, TTTTTTTTTTTTTTTTTTTTTTT=0.0839, TTTTTTTTTTTTTTTTTTTTTTTT=0.0036, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0036, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.108532	0.61606	0.275408	32
African	Sub	10	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	0	0	0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	10	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	0	0	0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	8	TTTTTTTTTTTTTTTTTTTT=0.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.2, TTTTTTTTTTTTTTTTTTTTTT=0.8, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	0.25	0.75	0.0	3

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
Allele Frequency Aggregator	Total	Global	4442	(T)₂₀=0.1297	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1909, dupTT=0.5867, dupTTT=0.0835, dup(T)₄=0.0036, dup(T)₅=0.0036, dup(T)₆=0.0000, dup(T)₉=0.0020
Allele Frequency Aggregator	European	Sub	4424	(T)₂₀=0.1279	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1912, dupTT=0.5877, dupTTT=0.0839, dup(T)₄=0.0036, dup(T)₅=0.0036, dup(T)₆=0.0000, dup(T)₉=0.0020
Allele Frequency Aggregator	African	Sub	10	(T)₂₀=1.0	del(T)₈=0.0, del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₉=0.0
Allele Frequency Aggregator	Other	Sub	8	(T)₂₀=0.0	del(T)₈=0.0, del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.2, dupTT=0.8, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₉=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₀=0	del(T)₈=0, del(T)₇=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₉=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₂₀=0	del(T)₈=0, del(T)₇=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₉=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₀=0	del(T)₈=0, del(T)₇=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₉=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₀=0	del(T)₈=0, del(T)₇=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₉=0

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 11	NC_000011.10:g.78470895_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470896_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470898_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470899_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470900_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470901_78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470902del
GRCh38.p14 chr 11	NC_000011.10:g.78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470901_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470900_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470899_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470898_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470897_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470896_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470895_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470894_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470892_78470902dup
GRCh38.p14 chr 11	NC_000011.10:g.78470886_78470902dup
GRCh37.p13 chr 11	NC_000011.9:g.78181941_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181942_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181944_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181945_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181946_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181947_78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181948del
GRCh37.p13 chr 11	NC_000011.9:g.78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181947_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181946_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181945_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181944_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181943_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181942_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181941_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181940_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181938_78181948dup
GRCh37.p13 chr 11	NC_000011.9:g.78181932_78181948dup
NARS2 RefSeqGene	NG_042046.1:g.108975_108982del
NARS2 RefSeqGene	NG_042046.1:g.108976_108982del
NARS2 RefSeqGene	NG_042046.1:g.108978_108982del
NARS2 RefSeqGene	NG_042046.1:g.108979_108982del
NARS2 RefSeqGene	NG_042046.1:g.108980_108982del
NARS2 RefSeqGene	NG_042046.1:g.108981_108982del
NARS2 RefSeqGene	NG_042046.1:g.108982del
NARS2 RefSeqGene	NG_042046.1:g.108982dup
NARS2 RefSeqGene	NG_042046.1:g.108981_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108980_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108979_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108978_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108977_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108976_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108975_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108974_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108972_108982dup
NARS2 RefSeqGene	NG_042046.1:g.108966_108982dup

Gene: NARS2, asparaginyl-tRNA synthetase 2, mitochondrial (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NARS2 transcript variant 2	NM_001243251.2:c.279-1577… NM_001243251.2:c.279-1577_279-1570del	N/A	Intron Variant
NARS2 transcript variant 1	NM_024678.6:c.960-1577_96… NM_024678.6:c.960-1577_960-1570del	N/A	Intron Variant
NARS2 transcript variant X1	XM_011545253.3:c.960-1577… XM_011545253.3:c.960-1577_960-1570del	N/A	Intron Variant
NARS2 transcript variant X2	XM_047427591.1:c.960-1577… XM_047427591.1:c.960-1577_960-1570del	N/A	Intron Variant
NARS2 transcript variant X3	XM_047427592.1:c.960-1577… XM_047427592.1:c.960-1577_960-1570del	N/A	Intron Variant
NARS2 transcript variant X4	XM_047427593.1:c.960-1577… XM_047427593.1:c.960-1577_960-1570del	N/A	Intron Variant
NARS2 transcript variant X5	XM_047427594.1:c.955-1577… XM_047427594.1:c.955-1577_955-1570del	N/A	Intron Variant
NARS2 transcript variant X6	XM_047427595.1:c.922-1577… XM_047427595.1:c.922-1577_922-1570del	N/A	Intron Variant
NARS2 transcript variant X7	XM_017018302.3:c.	N/A	Genic Downstream Transcript Variant

Gene: LOC105369403, uncharacterized LOC105369403 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105369403 transcript variant X1	XR_007062797.1:n.	N/A	Non Coding Transcript Variant
LOC105369403 transcript variant X2	XR_007062798.1:n.	N/A	Non Coding Transcript 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)₂₀=	del(T)₈	del(T)₇	del(T)₅	del(T)₄	delTTT	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)₁₁	dup(T)₁₇
GRCh38.p14 chr 11	NC_000011.10:g.78470883_78470902=	NC_000011.10:g.78470895_78470902del	NC_000011.10:g.78470896_78470902del	NC_000011.10:g.78470898_78470902del	NC_000011.10:g.78470899_78470902del	NC_000011.10:g.78470900_78470902del	NC_000011.10:g.78470901_78470902del	NC_000011.10:g.78470902del	NC_000011.10:g.78470902dup	NC_000011.10:g.78470901_78470902dup	NC_000011.10:g.78470900_78470902dup	NC_000011.10:g.78470899_78470902dup	NC_000011.10:g.78470898_78470902dup	NC_000011.10:g.78470897_78470902dup	NC_000011.10:g.78470896_78470902dup	NC_000011.10:g.78470895_78470902dup	NC_000011.10:g.78470894_78470902dup	NC_000011.10:g.78470892_78470902dup	NC_000011.10:g.78470886_78470902dup
GRCh37.p13 chr 11	NC_000011.9:g.78181929_78181948=	NC_000011.9:g.78181941_78181948del	NC_000011.9:g.78181942_78181948del	NC_000011.9:g.78181944_78181948del	NC_000011.9:g.78181945_78181948del	NC_000011.9:g.78181946_78181948del	NC_000011.9:g.78181947_78181948del	NC_000011.9:g.78181948del	NC_000011.9:g.78181948dup	NC_000011.9:g.78181947_78181948dup	NC_000011.9:g.78181946_78181948dup	NC_000011.9:g.78181945_78181948dup	NC_000011.9:g.78181944_78181948dup	NC_000011.9:g.78181943_78181948dup	NC_000011.9:g.78181942_78181948dup	NC_000011.9:g.78181941_78181948dup	NC_000011.9:g.78181940_78181948dup	NC_000011.9:g.78181938_78181948dup	NC_000011.9:g.78181932_78181948dup
NARS2 RefSeqGene	NG_042046.1:g.108963_108982=	NG_042046.1:g.108975_108982del	NG_042046.1:g.108976_108982del	NG_042046.1:g.108978_108982del	NG_042046.1:g.108979_108982del	NG_042046.1:g.108980_108982del	NG_042046.1:g.108981_108982del	NG_042046.1:g.108982del	NG_042046.1:g.108982dup	NG_042046.1:g.108981_108982dup	NG_042046.1:g.108980_108982dup	NG_042046.1:g.108979_108982dup	NG_042046.1:g.108978_108982dup	NG_042046.1:g.108977_108982dup	NG_042046.1:g.108976_108982dup	NG_042046.1:g.108975_108982dup	NG_042046.1:g.108974_108982dup	NG_042046.1:g.108972_108982dup	NG_042046.1:g.108966_108982dup
NARS2 transcript variant 2	NM_001243251.1:c.279-1570=	NM_001243251.1:c.279-1577_279-1570del	NM_001243251.1:c.279-1576_279-1570del	NM_001243251.1:c.279-1574_279-1570del	NM_001243251.1:c.279-1573_279-1570del	NM_001243251.1:c.279-1572_279-1570del	NM_001243251.1:c.279-1571_279-1570del	NM_001243251.1:c.279-1570del	NM_001243251.1:c.279-1570dup	NM_001243251.1:c.279-1571_279-1570dup	NM_001243251.1:c.279-1572_279-1570dup	NM_001243251.1:c.279-1573_279-1570dup	NM_001243251.1:c.279-1574_279-1570dup	NM_001243251.1:c.279-1575_279-1570dup	NM_001243251.1:c.279-1576_279-1570dup	NM_001243251.1:c.279-1577_279-1570dup	NM_001243251.1:c.279-1578_279-1570dup	NM_001243251.1:c.279-1580_279-1570dup	NM_001243251.1:c.279-1586_279-1570dup
NARS2 transcript variant 2	NM_001243251.2:c.279-1570=	NM_001243251.2:c.279-1577_279-1570del	NM_001243251.2:c.279-1576_279-1570del	NM_001243251.2:c.279-1574_279-1570del	NM_001243251.2:c.279-1573_279-1570del	NM_001243251.2:c.279-1572_279-1570del	NM_001243251.2:c.279-1571_279-1570del	NM_001243251.2:c.279-1570del	NM_001243251.2:c.279-1570dup	NM_001243251.2:c.279-1571_279-1570dup	NM_001243251.2:c.279-1572_279-1570dup	NM_001243251.2:c.279-1573_279-1570dup	NM_001243251.2:c.279-1574_279-1570dup	NM_001243251.2:c.279-1575_279-1570dup	NM_001243251.2:c.279-1576_279-1570dup	NM_001243251.2:c.279-1577_279-1570dup	NM_001243251.2:c.279-1578_279-1570dup	NM_001243251.2:c.279-1580_279-1570dup	NM_001243251.2:c.279-1586_279-1570dup
NARS2 transcript variant 1	NM_024678.5:c.960-1570=	NM_024678.5:c.960-1577_960-1570del	NM_024678.5:c.960-1576_960-1570del	NM_024678.5:c.960-1574_960-1570del	NM_024678.5:c.960-1573_960-1570del	NM_024678.5:c.960-1572_960-1570del	NM_024678.5:c.960-1571_960-1570del	NM_024678.5:c.960-1570del	NM_024678.5:c.960-1570dup	NM_024678.5:c.960-1571_960-1570dup	NM_024678.5:c.960-1572_960-1570dup	NM_024678.5:c.960-1573_960-1570dup	NM_024678.5:c.960-1574_960-1570dup	NM_024678.5:c.960-1575_960-1570dup	NM_024678.5:c.960-1576_960-1570dup	NM_024678.5:c.960-1577_960-1570dup	NM_024678.5:c.960-1578_960-1570dup	NM_024678.5:c.960-1580_960-1570dup	NM_024678.5:c.960-1586_960-1570dup
NARS2 transcript variant 1	NM_024678.6:c.960-1570=	NM_024678.6:c.960-1577_960-1570del	NM_024678.6:c.960-1576_960-1570del	NM_024678.6:c.960-1574_960-1570del	NM_024678.6:c.960-1573_960-1570del	NM_024678.6:c.960-1572_960-1570del	NM_024678.6:c.960-1571_960-1570del	NM_024678.6:c.960-1570del	NM_024678.6:c.960-1570dup	NM_024678.6:c.960-1571_960-1570dup	NM_024678.6:c.960-1572_960-1570dup	NM_024678.6:c.960-1573_960-1570dup	NM_024678.6:c.960-1574_960-1570dup	NM_024678.6:c.960-1575_960-1570dup	NM_024678.6:c.960-1576_960-1570dup	NM_024678.6:c.960-1577_960-1570dup	NM_024678.6:c.960-1578_960-1570dup	NM_024678.6:c.960-1580_960-1570dup	NM_024678.6:c.960-1586_960-1570dup
NARS2 transcript variant X1	XM_011545253.3:c.960-1570=	XM_011545253.3:c.960-1577_960-1570del	XM_011545253.3:c.960-1576_960-1570del	XM_011545253.3:c.960-1574_960-1570del	XM_011545253.3:c.960-1573_960-1570del	XM_011545253.3:c.960-1572_960-1570del	XM_011545253.3:c.960-1571_960-1570del	XM_011545253.3:c.960-1570del	XM_011545253.3:c.960-1570dup	XM_011545253.3:c.960-1571_960-1570dup	XM_011545253.3:c.960-1572_960-1570dup	XM_011545253.3:c.960-1573_960-1570dup	XM_011545253.3:c.960-1574_960-1570dup	XM_011545253.3:c.960-1575_960-1570dup	XM_011545253.3:c.960-1576_960-1570dup	XM_011545253.3:c.960-1577_960-1570dup	XM_011545253.3:c.960-1578_960-1570dup	XM_011545253.3:c.960-1580_960-1570dup	XM_011545253.3:c.960-1586_960-1570dup
NARS2 transcript variant X2	XM_047427591.1:c.960-1570=	XM_047427591.1:c.960-1577_960-1570del	XM_047427591.1:c.960-1576_960-1570del	XM_047427591.1:c.960-1574_960-1570del	XM_047427591.1:c.960-1573_960-1570del	XM_047427591.1:c.960-1572_960-1570del	XM_047427591.1:c.960-1571_960-1570del	XM_047427591.1:c.960-1570del	XM_047427591.1:c.960-1570dup	XM_047427591.1:c.960-1571_960-1570dup	XM_047427591.1:c.960-1572_960-1570dup	XM_047427591.1:c.960-1573_960-1570dup	XM_047427591.1:c.960-1574_960-1570dup	XM_047427591.1:c.960-1575_960-1570dup	XM_047427591.1:c.960-1576_960-1570dup	XM_047427591.1:c.960-1577_960-1570dup	XM_047427591.1:c.960-1578_960-1570dup	XM_047427591.1:c.960-1580_960-1570dup	XM_047427591.1:c.960-1586_960-1570dup
NARS2 transcript variant X3	XM_047427592.1:c.960-1570=	XM_047427592.1:c.960-1577_960-1570del	XM_047427592.1:c.960-1576_960-1570del	XM_047427592.1:c.960-1574_960-1570del	XM_047427592.1:c.960-1573_960-1570del	XM_047427592.1:c.960-1572_960-1570del	XM_047427592.1:c.960-1571_960-1570del	XM_047427592.1:c.960-1570del	XM_047427592.1:c.960-1570dup	XM_047427592.1:c.960-1571_960-1570dup	XM_047427592.1:c.960-1572_960-1570dup	XM_047427592.1:c.960-1573_960-1570dup	XM_047427592.1:c.960-1574_960-1570dup	XM_047427592.1:c.960-1575_960-1570dup	XM_047427592.1:c.960-1576_960-1570dup	XM_047427592.1:c.960-1577_960-1570dup	XM_047427592.1:c.960-1578_960-1570dup	XM_047427592.1:c.960-1580_960-1570dup	XM_047427592.1:c.960-1586_960-1570dup
NARS2 transcript variant X4	XM_047427593.1:c.960-1570=	XM_047427593.1:c.960-1577_960-1570del	XM_047427593.1:c.960-1576_960-1570del	XM_047427593.1:c.960-1574_960-1570del	XM_047427593.1:c.960-1573_960-1570del	XM_047427593.1:c.960-1572_960-1570del	XM_047427593.1:c.960-1571_960-1570del	XM_047427593.1:c.960-1570del	XM_047427593.1:c.960-1570dup	XM_047427593.1:c.960-1571_960-1570dup	XM_047427593.1:c.960-1572_960-1570dup	XM_047427593.1:c.960-1573_960-1570dup	XM_047427593.1:c.960-1574_960-1570dup	XM_047427593.1:c.960-1575_960-1570dup	XM_047427593.1:c.960-1576_960-1570dup	XM_047427593.1:c.960-1577_960-1570dup	XM_047427593.1:c.960-1578_960-1570dup	XM_047427593.1:c.960-1580_960-1570dup	XM_047427593.1:c.960-1586_960-1570dup
NARS2 transcript variant X5	XM_047427594.1:c.955-1570=	XM_047427594.1:c.955-1577_955-1570del	XM_047427594.1:c.955-1576_955-1570del	XM_047427594.1:c.955-1574_955-1570del	XM_047427594.1:c.955-1573_955-1570del	XM_047427594.1:c.955-1572_955-1570del	XM_047427594.1:c.955-1571_955-1570del	XM_047427594.1:c.955-1570del	XM_047427594.1:c.955-1570dup	XM_047427594.1:c.955-1571_955-1570dup	XM_047427594.1:c.955-1572_955-1570dup	XM_047427594.1:c.955-1573_955-1570dup	XM_047427594.1:c.955-1574_955-1570dup	XM_047427594.1:c.955-1575_955-1570dup	XM_047427594.1:c.955-1576_955-1570dup	XM_047427594.1:c.955-1577_955-1570dup	XM_047427594.1:c.955-1578_955-1570dup	XM_047427594.1:c.955-1580_955-1570dup	XM_047427594.1:c.955-1586_955-1570dup
NARS2 transcript variant X6	XM_047427595.1:c.922-1570=	XM_047427595.1:c.922-1577_922-1570del	XM_047427595.1:c.922-1576_922-1570del	XM_047427595.1:c.922-1574_922-1570del	XM_047427595.1:c.922-1573_922-1570del	XM_047427595.1:c.922-1572_922-1570del	XM_047427595.1:c.922-1571_922-1570del	XM_047427595.1:c.922-1570del	XM_047427595.1:c.922-1570dup	XM_047427595.1:c.922-1571_922-1570dup	XM_047427595.1:c.922-1572_922-1570dup	XM_047427595.1:c.922-1573_922-1570dup	XM_047427595.1:c.922-1574_922-1570dup	XM_047427595.1:c.922-1575_922-1570dup	XM_047427595.1:c.922-1576_922-1570dup	XM_047427595.1:c.922-1577_922-1570dup	XM_047427595.1:c.922-1578_922-1570dup	XM_047427595.1:c.922-1580_922-1570dup	XM_047427595.1:c.922-1586_922-1570dup

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#.

60 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80830409	Oct 12, 2018 (152)
2	HGSV	ss83889371	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss95573756	Oct 12, 2018 (152)
4	PJP	ss294711241	May 09, 2011 (137)
5	PJP	ss294711242	May 09, 2011 (137)
6	BILGI_BIOE	ss666541028	Apr 25, 2013 (138)
7	EVA_UK10K_ALSPAC	ss1707169047	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1707169048	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1707169339	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1707169342	Apr 01, 2015 (144)
11	SWEGEN	ss3008393936	Nov 08, 2017 (151)
12	SWEGEN	ss3008393937	Nov 08, 2017 (151)
13	SWEGEN	ss3008393938	Nov 08, 2017 (151)
14	SWEGEN	ss3008393939	Nov 08, 2017 (151)
15	URBANLAB	ss3649647969	Oct 12, 2018 (152)
16	EVA_DECODE	ss3692141557	Jul 13, 2019 (153)
17	EVA_DECODE	ss3692141558	Jul 13, 2019 (153)
18	EVA_DECODE	ss3692141559	Jul 13, 2019 (153)
19	EVA_DECODE	ss3692141560	Jul 13, 2019 (153)
20	PACBIO	ss3786999420	Jul 13, 2019 (153)
21	PACBIO	ss3792132666	Jul 13, 2019 (153)
22	PACBIO	ss3792132667	Jul 13, 2019 (153)
23	PACBIO	ss3797015024	Jul 13, 2019 (153)
24	PACBIO	ss3797015025	Jul 13, 2019 (153)
25	EVA	ss3832714972	Apr 26, 2020 (154)
26	GNOMAD	ss4238353462	Apr 26, 2021 (155)
27	GNOMAD	ss4238353463	Apr 26, 2021 (155)
28	GNOMAD	ss4238353464	Apr 26, 2021 (155)
29	GNOMAD	ss4238353465	Apr 26, 2021 (155)
30	GNOMAD	ss4238353466	Apr 26, 2021 (155)
31	GNOMAD	ss4238353467	Apr 26, 2021 (155)
32	GNOMAD	ss4238353468	Apr 26, 2021 (155)
33	GNOMAD	ss4238353469	Apr 26, 2021 (155)
34	GNOMAD	ss4238353470	Apr 26, 2021 (155)
35	GNOMAD	ss4238353471	Apr 26, 2021 (155)
36	GNOMAD	ss4238353473	Apr 26, 2021 (155)
37	GNOMAD	ss4238353474	Apr 26, 2021 (155)
38	GNOMAD	ss4238353475	Apr 26, 2021 (155)
39	GNOMAD	ss4238353476	Apr 26, 2021 (155)
40	GNOMAD	ss4238353477	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5202828274	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5202828275	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5202828276	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5202828277	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5288067949	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5288067950	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5288067951	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5288067952	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5288067953	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5483158491	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5483158492	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5483158493	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5750978324	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5750978325	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5750978326	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5750978327	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5750978329	Oct 16, 2022 (156)
58	EVA	ss5836903761	Oct 16, 2022 (156)
59	EVA	ss5836903762	Oct 16, 2022 (156)
60	EVA	ss5920699905	Oct 16, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30277751 (NC_000011.9:78181928::TTT 528/3854) Row 30277752 (NC_000011.9:78181928::TT 3326/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30277751 (NC_000011.9:78181928::TTT 528/3854) Row 30277752 (NC_000011.9:78181928::TT 3326/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 385052525 (NC_000011.10:78470882::T 33243/124094) Row 385052526 (NC_000011.10:78470882::TT 73302/124170) Row 385052527 (NC_000011.10:78470882::TTT 13036/123988)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 60797581 (NC_000011.9:78181928::T 7179/16666) Row 60797582 (NC_000011.9:78181928::TT 9128/16666) Row 60797583 (NC_000011.9:78181928:TTTTT: 5/16666)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 60797581 (NC_000011.9:78181928::T 7179/16666) Row 60797582 (NC_000011.9:78181928::TT 9128/16666) Row 60797583 (NC_000011.9:78181928:TTTTT: 5/16666)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 60797581 (NC_000011.9:78181928::T 7179/16666) Row 60797582 (NC_000011.9:78181928::TT 9128/16666) Row 60797583 (NC_000011.9:78181928:TTTTT: 5/16666)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 60797581 (NC_000011.9:78181928::T 7179/16666) Row 60797582 (NC_000011.9:78181928::TT 9128/16666) Row 60797583 (NC_000011.9:78181928:TTTTT: 5/16666)...	-	Apr 26, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 84815428 (NC_000011.10:78470882::T 12200/28256) Row 84815429 (NC_000011.10:78470882::TT 15639/28256) Row 84815430 (NC_000011.10:78470882::TTT 72/28256)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 84815428 (NC_000011.10:78470882::T 12200/28256) Row 84815429 (NC_000011.10:78470882::TT 15639/28256) Row 84815430 (NC_000011.10:78470882::TTT 72/28256)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 84815428 (NC_000011.10:78470882::T 12200/28256) Row 84815429 (NC_000011.10:78470882::TT 15639/28256) Row 84815430 (NC_000011.10:78470882::TTT 72/28256)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 84815428 (NC_000011.10:78470882::T 12200/28256) Row 84815429 (NC_000011.10:78470882::TT 15639/28256) Row 84815430 (NC_000011.10:78470882::TTT 72/28256)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 84815428 (NC_000011.10:78470882::T 12200/28256) Row 84815429 (NC_000011.10:78470882::TT 15639/28256) Row 84815430 (NC_000011.10:78470882::TTT 72/28256)...	-	Oct 16, 2022 (156)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30277751 (NC_000011.9:78181928::TTT 525/3708) Row 30277752 (NC_000011.9:78181928::TT 3183/3708)	-	Oct 12, 2018 (152)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30277751 (NC_000011.9:78181928::TTT 525/3708) Row 30277752 (NC_000011.9:78181928::TT 3183/3708)	-	Oct 12, 2018 (152)
89	ALFA	NC_000011.10 - 78470883	Apr 26, 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)
rs67863153	Feb 27, 2009 (130)
rs71895412	May 11, 2012 (137)
rs72295104	May 11, 2012 (137)
rs72431740	May 11, 2012 (137)
rs143190895	Sep 17, 2011 (135)
rs146199164	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5202828276	NC_000011.9:78181928:TTTTT:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4238353477, ss5750978327	NC_000011.10:78470882:TTTTT:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4238353476	NC_000011.10:78470882:TTTT:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4238353475	NC_000011.10:78470882:TTT:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4238353474	NC_000011.10:78470882:TT:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4238353473, ss5920699905	NC_000011.10:78470882:T:	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss666541028, ss3008393936, ss3792132666, ss3797015024, ss5202828274	NC_000011.9:78181928::T	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3692141557, ss4238353462, ss5288067950, ss5483158491, ss5750978324	NC_000011.10:78470882::T	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss294711241	NC_000011.8:77859577::TT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss294711242	NC_000011.8:77859595::TT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1707169048, ss1707169342, ss3008393937, ss3786999420, ss3792132667, ss3797015025, ss3832714972, ss5202828275, ss5836903761	NC_000011.9:78181928::TT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3649647969, ss3692141558, ss4238353463, ss5288067949, ss5483158492, ss5750978325	NC_000011.10:78470882::TT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss80830409, ss95573756	NT_167190.1:23487743::TT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1707169047, ss1707169339, ss3008393938, ss5202828277, ss5836903762	NC_000011.9:78181928::TTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3692141559, ss4238353464, ss5288067951, ss5483158493, ss5750978326	NC_000011.10:78470882::TTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3008393939	NC_000011.9:78181928::TTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353465, ss5288067953, ss5750978329	NC_000011.10:78470882::TTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353466, ss5288067952	NC_000011.10:78470882::TTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss83889371	NT_167190.1:23487743::TTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353467	NC_000011.10:78470882::TTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353468	NC_000011.10:78470882::TTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3692141560	NC_000011.10:78470882::TTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353469	NC_000011.10:78470882::TTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10246712383	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353470	NC_000011.10:78470882::TTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4238353471	NC_000011.10:78470882::TTTTTTTTTTT… NC_000011.10:78470882::TTTTTTTTTTTTTTTTT	NC_000011.10:78470882:TTTTTTTTTTTT… NC_000011.10:78470882:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs67863152

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

rs67863152