Name: rs35304758
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.

rs35304758

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:57034050-57034068 (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(A)₈ / del(A)₆ / del(A)₄ / delA…
del(A)₈ / del(A)₆ / del(A)₄ / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₁₀ / dup(A)₁₃ / ins(A)₃₅
Variation Type: Indel Insertion and Deletion
Frequency: dupAA=0.4856 (2432/5008, 1000G)
del(A)₈=0.000 (0/220, ALFA)
del(A)₆=0.000 (0/220, ALFA) (+ 10 more)
del(A)₄=0.000 (0/220, ALFA)
delAA=0.000 (0/220, ALFA)
delA=0.000 (0/220, ALFA)
dupA=0.000 (0/220, ALFA)
dupAA=0.000 (0/220, ALFA)
dupAAA=0.000 (0/220, ALFA)
dup(A)₄=0.000 (0/220, ALFA)
dup(A)₅=0.000 (0/220, ALFA)
dup(A)₆=0.000 (0/220, ALFA)
dup(A)₇=0.000 (0/220, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IGFBP7 : 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	220	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	136	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	64	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	62	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	8	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	12	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAA=0.4856
1000Genomes	African	Sub	1322	- No frequency provided	dupAA=0.5484
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAA=0.4990
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAA=0.3608
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAA=0.484
1000Genomes	American	Sub	694	- No frequency provided	dupAA=0.530
Allele Frequency Aggregator	Total	Global	220	(A)₁₉=1.000	del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	European	Sub	136	(A)₁₉=1.000	del(A)₈=0.000, del(A)₆=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	African	Sub	64	(A)₁₉=1.00	del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Other	Sub	12	(A)₁₉=1.00	del(A)₈=0.00, del(A)₆=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	8	(A)₁₉=1.0	del(A)₈=0.0, del(A)₆=0.0, del(A)₄=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0, dup(A)₇=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₆=0, del(A)₄=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₆=0, del(A)₄=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₆=0, del(A)₄=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=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 4	NC_000004.12:g.57034061_57034068del
GRCh38.p14 chr 4	NC_000004.12:g.57034063_57034068del
GRCh38.p14 chr 4	NC_000004.12:g.57034065_57034068del
GRCh38.p14 chr 4	NC_000004.12:g.57034067_57034068del
GRCh38.p14 chr 4	NC_000004.12:g.57034068del
GRCh38.p14 chr 4	NC_000004.12:g.57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034067_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034066_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034065_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034064_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034063_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034062_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034061_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034059_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034056_57034068dup
GRCh38.p14 chr 4	NC_000004.12:g.57034068_57034069insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 4	NC_000004.11:g.57900227_57900234del
GRCh37.p13 chr 4	NC_000004.11:g.57900229_57900234del
GRCh37.p13 chr 4	NC_000004.11:g.57900231_57900234del
GRCh37.p13 chr 4	NC_000004.11:g.57900233_57900234del
GRCh37.p13 chr 4	NC_000004.11:g.57900234del
GRCh37.p13 chr 4	NC_000004.11:g.57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900233_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900232_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900231_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900230_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900229_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900228_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900227_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900225_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900222_57900234dup
GRCh37.p13 chr 4	NC_000004.11:g.57900234_57900235insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.81329_81336del
IGFBP7 RefSeqGene	NG_031877.1:g.81331_81336del
IGFBP7 RefSeqGene	NG_031877.1:g.81333_81336del
IGFBP7 RefSeqGene	NG_031877.1:g.81335_81336del
IGFBP7 RefSeqGene	NG_031877.1:g.81336del
IGFBP7 RefSeqGene	NG_031877.1:g.81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81335_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81334_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81333_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81332_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81331_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81330_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81329_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81327_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81324_81336dup
IGFBP7 RefSeqGene	NG_031877.1:g.81336_81337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: IGFBP7, insulin like growth factor binding protein 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IGFBP7 transcript variant 2	NM_001253835.2:c.586-746_… NM_001253835.2:c.586-746_586-739del	N/A	Intron Variant
IGFBP7 transcript variant 1	NM_001553.3:c.586-746_586… NM_001553.3:c.586-746_586-739del	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	(A)₁₉=	del(A)₈	del(A)₆	del(A)₄	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₁₀	dup(A)₁₃	ins(A)₃₅
GRCh38.p14 chr 4	NC_000004.12:g.57034050_57034068=	NC_000004.12:g.57034061_57034068del	NC_000004.12:g.57034063_57034068del	NC_000004.12:g.57034065_57034068del	NC_000004.12:g.57034067_57034068del	NC_000004.12:g.57034068del	NC_000004.12:g.57034068dup	NC_000004.12:g.57034067_57034068dup	NC_000004.12:g.57034066_57034068dup	NC_000004.12:g.57034065_57034068dup	NC_000004.12:g.57034064_57034068dup	NC_000004.12:g.57034063_57034068dup	NC_000004.12:g.57034062_57034068dup	NC_000004.12:g.57034061_57034068dup	NC_000004.12:g.57034059_57034068dup	NC_000004.12:g.57034056_57034068dup	NC_000004.12:g.57034068_57034069insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 4	NC_000004.11:g.57900216_57900234=	NC_000004.11:g.57900227_57900234del	NC_000004.11:g.57900229_57900234del	NC_000004.11:g.57900231_57900234del	NC_000004.11:g.57900233_57900234del	NC_000004.11:g.57900234del	NC_000004.11:g.57900234dup	NC_000004.11:g.57900233_57900234dup	NC_000004.11:g.57900232_57900234dup	NC_000004.11:g.57900231_57900234dup	NC_000004.11:g.57900230_57900234dup	NC_000004.11:g.57900229_57900234dup	NC_000004.11:g.57900228_57900234dup	NC_000004.11:g.57900227_57900234dup	NC_000004.11:g.57900225_57900234dup	NC_000004.11:g.57900222_57900234dup	NC_000004.11:g.57900234_57900235insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.81318_81336=	NG_031877.1:g.81329_81336del	NG_031877.1:g.81331_81336del	NG_031877.1:g.81333_81336del	NG_031877.1:g.81335_81336del	NG_031877.1:g.81336del	NG_031877.1:g.81336dup	NG_031877.1:g.81335_81336dup	NG_031877.1:g.81334_81336dup	NG_031877.1:g.81333_81336dup	NG_031877.1:g.81332_81336dup	NG_031877.1:g.81331_81336dup	NG_031877.1:g.81330_81336dup	NG_031877.1:g.81329_81336dup	NG_031877.1:g.81327_81336dup	NG_031877.1:g.81324_81336dup	NG_031877.1:g.81336_81337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 transcript variant 2	NM_001253835.1:c.586-739=	NM_001253835.1:c.586-746_586-739del	NM_001253835.1:c.586-744_586-739del	NM_001253835.1:c.586-742_586-739del	NM_001253835.1:c.586-740_586-739del	NM_001253835.1:c.586-739del	NM_001253835.1:c.586-739dup	NM_001253835.1:c.586-740_586-739dup	NM_001253835.1:c.586-741_586-739dup	NM_001253835.1:c.586-742_586-739dup	NM_001253835.1:c.586-743_586-739dup	NM_001253835.1:c.586-744_586-739dup	NM_001253835.1:c.586-745_586-739dup	NM_001253835.1:c.586-746_586-739dup	NM_001253835.1:c.586-748_586-739dup	NM_001253835.1:c.586-751_586-739dup	NM_001253835.1:c.586-739_586-738insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 transcript variant 2	NM_001253835.2:c.586-739=	NM_001253835.2:c.586-746_586-739del	NM_001253835.2:c.586-744_586-739del	NM_001253835.2:c.586-742_586-739del	NM_001253835.2:c.586-740_586-739del	NM_001253835.2:c.586-739del	NM_001253835.2:c.586-739dup	NM_001253835.2:c.586-740_586-739dup	NM_001253835.2:c.586-741_586-739dup	NM_001253835.2:c.586-742_586-739dup	NM_001253835.2:c.586-743_586-739dup	NM_001253835.2:c.586-744_586-739dup	NM_001253835.2:c.586-745_586-739dup	NM_001253835.2:c.586-746_586-739dup	NM_001253835.2:c.586-748_586-739dup	NM_001253835.2:c.586-751_586-739dup	NM_001253835.2:c.586-739_586-738insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 transcript variant 1	NM_001553.2:c.586-739=	NM_001553.2:c.586-746_586-739del	NM_001553.2:c.586-744_586-739del	NM_001553.2:c.586-742_586-739del	NM_001553.2:c.586-740_586-739del	NM_001553.2:c.586-739del	NM_001553.2:c.586-739dup	NM_001553.2:c.586-740_586-739dup	NM_001553.2:c.586-741_586-739dup	NM_001553.2:c.586-742_586-739dup	NM_001553.2:c.586-743_586-739dup	NM_001553.2:c.586-744_586-739dup	NM_001553.2:c.586-745_586-739dup	NM_001553.2:c.586-746_586-739dup	NM_001553.2:c.586-748_586-739dup	NM_001553.2:c.586-751_586-739dup	NM_001553.2:c.586-739_586-738insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 transcript variant 1	NM_001553.3:c.586-739=	NM_001553.3:c.586-746_586-739del	NM_001553.3:c.586-744_586-739del	NM_001553.3:c.586-742_586-739del	NM_001553.3:c.586-740_586-739del	NM_001553.3:c.586-739del	NM_001553.3:c.586-739dup	NM_001553.3:c.586-740_586-739dup	NM_001553.3:c.586-741_586-739dup	NM_001553.3:c.586-742_586-739dup	NM_001553.3:c.586-743_586-739dup	NM_001553.3:c.586-744_586-739dup	NM_001553.3:c.586-745_586-739dup	NM_001553.3:c.586-746_586-739dup	NM_001553.3:c.586-748_586-739dup	NM_001553.3:c.586-751_586-739dup	NM_001553.3:c.586-739_586-738insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83839521	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95355187	Feb 06, 2009 (130)
3	HUMANGENOME_JCVI	ss98910542	Feb 13, 2009 (130)
4	PJP	ss295166170	May 09, 2011 (135)
5	BILGI_BIOE	ss666258894	Apr 25, 2013 (138)
6	SSIP	ss947116175	Aug 21, 2014 (142)
7	1000GENOMES	ss1372191591	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1704164040	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1704164041	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1704164043	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1704164896	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1704164897	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1704164898	Apr 01, 2015 (144)
14	SWEGEN	ss2994705393	Nov 08, 2017 (151)
15	URBANLAB	ss3647730053	Oct 12, 2018 (152)
16	EVA_DECODE	ss3712059259	Jul 13, 2019 (153)
17	EVA_DECODE	ss3712059260	Jul 13, 2019 (153)
18	EVA_DECODE	ss3712059261	Jul 13, 2019 (153)
19	EVA_DECODE	ss3712059262	Jul 13, 2019 (153)
20	EVA_DECODE	ss3712059263	Jul 13, 2019 (153)
21	EVA_DECODE	ss3712059264	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3804936439	Jul 13, 2019 (153)
23	EVA	ss3828541515	Apr 26, 2020 (154)
24	GNOMAD	ss4111348900	Apr 26, 2021 (155)
25	GNOMAD	ss4111348901	Apr 26, 2021 (155)
26	GNOMAD	ss4111348902	Apr 26, 2021 (155)
27	GNOMAD	ss4111348903	Apr 26, 2021 (155)
28	GNOMAD	ss4111348904	Apr 26, 2021 (155)
29	GNOMAD	ss4111348905	Apr 26, 2021 (155)
30	GNOMAD	ss4111348906	Apr 26, 2021 (155)
31	GNOMAD	ss4111348907	Apr 26, 2021 (155)
32	GNOMAD	ss4111348908	Apr 26, 2021 (155)
33	GNOMAD	ss4111348909	Apr 26, 2021 (155)
34	GNOMAD	ss4111348910	Apr 26, 2021 (155)
35	GNOMAD	ss4111348912	Apr 26, 2021 (155)
36	GNOMAD	ss4111348913	Apr 26, 2021 (155)
37	GNOMAD	ss4111348914	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5165730307	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5165730308	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5165730309	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5165730310	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5165730311	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5259211721	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5259211722	Oct 13, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5259211723	Oct 13, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5259211724	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5259211725	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5259211726	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5457971306	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5457971307	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5457971308	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5457971309	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5457971310	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5700079612	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5700079613	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5700079614	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5700079615	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5700079617	Oct 13, 2022 (156)
59	EVA	ss5844001236	Oct 13, 2022 (156)
60	EVA	ss5844001237	Oct 13, 2022 (156)
61	1000Genomes	NC_000004.11 - 57900216	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3854) Row 11766981 (NC_000004.11:57900215::AAA 1903/3854) Row 11766982 (NC_000004.11:57900215::AA 1669/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3854) Row 11766981 (NC_000004.11:57900215::AAA 1903/3854) Row 11766982 (NC_000004.11:57900215::AA 1669/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3854) Row 11766981 (NC_000004.11:57900215::AAA 1903/3854) Row 11766982 (NC_000004.11:57900215::AA 1669/3854)	-	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149849145 (NC_000004.12:57034049::A 12947/89388) Row 149849146 (NC_000004.12:57034049::AA 37511/89184) Row 149849147 (NC_000004.12:57034049::AAA 21050/88978)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 23699614 (NC_000004.11:57900215::AA 4447/15768) Row 23699615 (NC_000004.11:57900215::AAA 3297/15768) Row 23699616 (NC_000004.11:57900215::A 5710/15768)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 23699614 (NC_000004.11:57900215::AA 4447/15768) Row 23699615 (NC_000004.11:57900215::AAA 3297/15768) Row 23699616 (NC_000004.11:57900215::A 5710/15768)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 23699614 (NC_000004.11:57900215::AA 4447/15768) Row 23699615 (NC_000004.11:57900215::AAA 3297/15768) Row 23699616 (NC_000004.11:57900215::A 5710/15768)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 23699614 (NC_000004.11:57900215::AA 4447/15768) Row 23699615 (NC_000004.11:57900215::AAA 3297/15768) Row 23699616 (NC_000004.11:57900215::A 5710/15768)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 23699614 (NC_000004.11:57900215::AA 4447/15768) Row 23699615 (NC_000004.11:57900215::AAA 3297/15768) Row 23699616 (NC_000004.11:57900215::A 5710/15768)...	-	Apr 26, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 33916716 (NC_000004.12:57034049::A 10417/28042) Row 33916717 (NC_000004.12:57034049::AAA 6240/28042) Row 33916718 (NC_000004.12:57034049::AA 8287/28042)...	-	Oct 13, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 33916716 (NC_000004.12:57034049::A 10417/28042) Row 33916717 (NC_000004.12:57034049::AAA 6240/28042) Row 33916718 (NC_000004.12:57034049::AA 8287/28042)...	-	Oct 13, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 33916716 (NC_000004.12:57034049::A 10417/28042) Row 33916717 (NC_000004.12:57034049::AAA 6240/28042) Row 33916718 (NC_000004.12:57034049::AA 8287/28042)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 33916716 (NC_000004.12:57034049::A 10417/28042) Row 33916717 (NC_000004.12:57034049::AAA 6240/28042) Row 33916718 (NC_000004.12:57034049::AA 8287/28042)...	-	Oct 13, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 33916716 (NC_000004.12:57034049::A 10417/28042) Row 33916717 (NC_000004.12:57034049::AAA 6240/28042) Row 33916718 (NC_000004.12:57034049::AA 8287/28042)...	-	Oct 13, 2022 (156)
89	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3708) Row 11766981 (NC_000004.11:57900215::AAA 1926/3708) Row 11766982 (NC_000004.11:57900215::AA 1489/3708)	-	Oct 12, 2018 (152)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3708) Row 11766981 (NC_000004.11:57900215::AAA 1926/3708) Row 11766982 (NC_000004.11:57900215::AA 1489/3708)	-	Oct 12, 2018 (152)
91	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11766980 (NC_000004.11:57900215::AAAA 268/3708) Row 11766981 (NC_000004.11:57900215::AAA 1926/3708) Row 11766982 (NC_000004.11:57900215::AA 1489/3708)	-	Oct 12, 2018 (152)
92	ALFA	NC_000004.12 - 57034050	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)
rs35488050	May 11, 2012 (137)
rs140462092	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4111348914	NC_000004.12:57034049:AAAAAA:	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4111348913	NC_000004.12:57034049:AA:	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss2994705393	NC_000004.11:57900215:A:	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3712059264, ss4111348912, ss5259211726, ss5457971309	NC_000004.12:57034049:A:	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss947116175, ss5165730309	NC_000004.11:57900215::A	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4111348900, ss5259211723, ss5457971307, ss5700079612	NC_000004.12:57034049::A	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3712059263	NC_000004.12:57034050::A	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss295166170	NC_000004.10:57594973::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
21143037, ss666258894, ss1372191591, ss1704164043, ss1704164898, ss3828541515, ss5165730307, ss5844001236	NC_000004.11:57900215::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3804936439, ss4111348901, ss5259211721, ss5457971310, ss5700079614	NC_000004.12:57034049::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3712059262	NC_000004.12:57034050::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss98910542	NT_022853.15:5240098::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss83839521	NT_022853.15:5240117::AA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss1704164041, ss1704164897, ss5165730308, ss5844001237	NC_000004.11:57900215::AAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348902, ss5259211725, ss5457971306, ss5700079613	NC_000004.12:57034049::AAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712059261	NC_000004.12:57034050::AAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1704164040, ss1704164896, ss5165730310	NC_000004.11:57900215::AAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3647730053, ss4111348903, ss5259211722, ss5457971308, ss5700079615	NC_000004.12:57034049::AAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712059260	NC_000004.12:57034050::AAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95355187	NT_022853.15:5240117::AAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5165730311	NC_000004.11:57900215::AAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348904, ss5259211724, ss5700079617	NC_000004.12:57034049::AAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712059259	NC_000004.12:57034050::AAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348905	NC_000004.12:57034049::AAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348906	NC_000004.12:57034049::AAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8389246165	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348907	NC_000004.12:57034049::AAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348908	NC_000004.12:57034049::AAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348909	NC_000004.12:57034049::AAAAAAAAAAA… NC_000004.12:57034049::AAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4111348910	NC_000004.12:57034049::AAAAAAAAAAA… NC_000004.12:57034049::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:57034049:AAAAAAAAAAAA… NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35304758

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

rs35304758