Name: rs370816490
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.

rs370816490

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:149402690-149402708 (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)₁₁ / del(A)₁₀ / del(A)₉ / de…
del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₇ / del(A)₆ / del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.0000 (0/8734, ALFA)
del(A)₁₀=0.0000 (0/8734, ALFA)
del(A)₉=0.0000 (0/8734, ALFA) (+ 13 more)
del(A)₇=0.0000 (0/8734, ALFA)
del(A)₆=0.0000 (0/8734, ALFA)
del(A)₅=0.0000 (0/8734, ALFA)
delAAA=0.0000 (0/8734, ALFA)
delAA=0.0000 (0/8734, ALFA)
delA=0.0000 (0/8734, ALFA)
dupA=0.0000 (0/8734, ALFA)
dupAA=0.0000 (0/8734, ALFA)
dupAAA=0.0000 (0/8734, ALFA)
dup(A)₄=0.0000 (0/8734, ALFA)
dup(A)₅=0.0000 (0/8734, ALFA)
dup(A)₆=0.0000 (0/8734, ALFA)
dupAA=0.078 (39/498, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IL17B : 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	HWEP
Total	Global	8734	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	6982	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	774	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=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	1.0	N/A
African Others	Sub	36	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
African American	Sub	738	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=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	1.0	N/A
Asian	Sub	90	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
East Asian	Sub	76	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
Other Asian	Sub	14	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
Latin American 1	Sub	62	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
Latin American 2	Sub	462	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=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	1.0	N/A
South Asian	Sub	78	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	1.0	N/A
Other	Sub	286	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=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	1.0	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
Allele Frequency Aggregator	Total	Global	8734	(A)₁₉=1.0000	del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	6982	(A)₁₉=1.0000	del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	774	(A)₁₉=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=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
Allele Frequency Aggregator	Latin American 2	Sub	462	(A)₁₉=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=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
Allele Frequency Aggregator	Other	Sub	286	(A)₁₉=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=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
Allele Frequency Aggregator	Asian	Sub	90	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=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
Allele Frequency Aggregator	South Asian	Sub	78	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=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
Allele Frequency Aggregator	Latin American 1	Sub	62	(A)₁₉=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=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
Northern Sweden	ACPOP	Study-wide	498	- No frequency provided	dupAA=0.078

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 5	NC_000005.10:g.149402698_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402699_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402700_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402702_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402703_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402704_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402706_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402707_149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402708del
GRCh38.p14 chr 5	NC_000005.10:g.149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402707_149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402706_149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402705_149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402704_149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402703_149402708dup
GRCh38.p14 chr 5	NC_000005.10:g.149402701_149402708dup
GRCh37.p13 chr 5	NC_000005.9:g.148782261_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782262_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782263_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782265_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782266_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782267_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782269_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782270_148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782271del
GRCh37.p13 chr 5	NC_000005.9:g.148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782270_148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782269_148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782268_148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782267_148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782266_148782271dup
GRCh37.p13 chr 5	NC_000005.9:g.148782264_148782271dup

Gene: IL17B, interleukin 17B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IL17B transcript variant 2	NM_001317987.2:c.-136+140… NM_001317987.2:c.-136+1408_-136+1418del	N/A	Intron Variant
IL17B transcript variant 1	NM_014443.3:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X2	XM_017009347.2:c.-407+140… XM_017009347.2:c.-407+1408_-407+1418del	N/A	Intron Variant
IL17B transcript variant X3	XM_017009348.2:c.-246+140… XM_017009348.2:c.-246+1408_-246+1418del	N/A	Intron Variant
IL17B transcript variant X1	XM_017009346.2:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X4	XM_047417104.1:c.	N/A	Genic Upstream 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	(A)₁₉=	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₇	del(A)₆	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₈
GRCh38.p14 chr 5	NC_000005.10:g.149402690_149402708=	NC_000005.10:g.149402698_149402708del	NC_000005.10:g.149402699_149402708del	NC_000005.10:g.149402700_149402708del	NC_000005.10:g.149402702_149402708del	NC_000005.10:g.149402703_149402708del	NC_000005.10:g.149402704_149402708del	NC_000005.10:g.149402706_149402708del	NC_000005.10:g.149402707_149402708del	NC_000005.10:g.149402708del	NC_000005.10:g.149402708dup	NC_000005.10:g.149402707_149402708dup	NC_000005.10:g.149402706_149402708dup	NC_000005.10:g.149402705_149402708dup	NC_000005.10:g.149402704_149402708dup	NC_000005.10:g.149402703_149402708dup	NC_000005.10:g.149402701_149402708dup
GRCh37.p13 chr 5	NC_000005.9:g.148782253_148782271=	NC_000005.9:g.148782261_148782271del	NC_000005.9:g.148782262_148782271del	NC_000005.9:g.148782263_148782271del	NC_000005.9:g.148782265_148782271del	NC_000005.9:g.148782266_148782271del	NC_000005.9:g.148782267_148782271del	NC_000005.9:g.148782269_148782271del	NC_000005.9:g.148782270_148782271del	NC_000005.9:g.148782271del	NC_000005.9:g.148782271dup	NC_000005.9:g.148782270_148782271dup	NC_000005.9:g.148782269_148782271dup	NC_000005.9:g.148782268_148782271dup	NC_000005.9:g.148782267_148782271dup	NC_000005.9:g.148782266_148782271dup	NC_000005.9:g.148782264_148782271dup
IL17B transcript variant 2	NM_001317987.2:c.-136+1418=	NM_001317987.2:c.-136+1408_-136+1418del	NM_001317987.2:c.-136+1409_-136+1418del	NM_001317987.2:c.-136+1410_-136+1418del	NM_001317987.2:c.-136+1412_-136+1418del	NM_001317987.2:c.-136+1413_-136+1418del	NM_001317987.2:c.-136+1414_-136+1418del	NM_001317987.2:c.-136+1416_-136+1418del	NM_001317987.2:c.-136+1417_-136+1418del	NM_001317987.2:c.-136+1418del	NM_001317987.2:c.-136+1418dup	NM_001317987.2:c.-136+1417_-136+1418dup	NM_001317987.2:c.-136+1416_-136+1418dup	NM_001317987.2:c.-136+1415_-136+1418dup	NM_001317987.2:c.-136+1414_-136+1418dup	NM_001317987.2:c.-136+1413_-136+1418dup	NM_001317987.2:c.-136+1411_-136+1418dup
IL17B transcript variant X2	XM_017009347.2:c.-407+1418=	XM_017009347.2:c.-407+1408_-407+1418del	XM_017009347.2:c.-407+1409_-407+1418del	XM_017009347.2:c.-407+1410_-407+1418del	XM_017009347.2:c.-407+1412_-407+1418del	XM_017009347.2:c.-407+1413_-407+1418del	XM_017009347.2:c.-407+1414_-407+1418del	XM_017009347.2:c.-407+1416_-407+1418del	XM_017009347.2:c.-407+1417_-407+1418del	XM_017009347.2:c.-407+1418del	XM_017009347.2:c.-407+1418dup	XM_017009347.2:c.-407+1417_-407+1418dup	XM_017009347.2:c.-407+1416_-407+1418dup	XM_017009347.2:c.-407+1415_-407+1418dup	XM_017009347.2:c.-407+1414_-407+1418dup	XM_017009347.2:c.-407+1413_-407+1418dup	XM_017009347.2:c.-407+1411_-407+1418dup
IL17B transcript variant X3	XM_017009348.2:c.-246+1418=	XM_017009348.2:c.-246+1408_-246+1418del	XM_017009348.2:c.-246+1409_-246+1418del	XM_017009348.2:c.-246+1410_-246+1418del	XM_017009348.2:c.-246+1412_-246+1418del	XM_017009348.2:c.-246+1413_-246+1418del	XM_017009348.2:c.-246+1414_-246+1418del	XM_017009348.2:c.-246+1416_-246+1418del	XM_017009348.2:c.-246+1417_-246+1418del	XM_017009348.2:c.-246+1418del	XM_017009348.2:c.-246+1418dup	XM_017009348.2:c.-246+1417_-246+1418dup	XM_017009348.2:c.-246+1416_-246+1418dup	XM_017009348.2:c.-246+1415_-246+1418dup	XM_017009348.2:c.-246+1414_-246+1418dup	XM_017009348.2:c.-246+1413_-246+1418dup	XM_017009348.2:c.-246+1411_-246+1418dup

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#.

47 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BILGI_BIOE	ss666332007	Apr 25, 2013 (138)
2	SSIP	ss947156181	Aug 21, 2014 (142)
3	SWEGEN	ss2997988609	Nov 08, 2017 (151)
4	SWEGEN	ss2997988610	Nov 08, 2017 (151)
5	EVA_DECODE	ss3715937943	Jul 13, 2019 (153)
6	EVA_DECODE	ss3715937944	Jul 13, 2019 (153)
7	EVA_DECODE	ss3715937945	Jul 13, 2019 (153)
8	EVA_DECODE	ss3715937946	Jul 13, 2019 (153)
9	ACPOP	ss3732919467	Jul 13, 2019 (153)
10	PACBIO	ss3785281345	Jul 13, 2019 (153)
11	EVA	ss3829563321	Apr 26, 2020 (154)
12	EVA	ss3838255644	Apr 26, 2020 (154)
13	EVA	ss3843698691	Apr 26, 2020 (154)
14	GNOMAD	ss4131532057	Apr 26, 2021 (155)
15	GNOMAD	ss4131532058	Apr 26, 2021 (155)
16	GNOMAD	ss4131532059	Apr 26, 2021 (155)
17	GNOMAD	ss4131532060	Apr 26, 2021 (155)
18	GNOMAD	ss4131532061	Apr 26, 2021 (155)
19	GNOMAD	ss4131532062	Apr 26, 2021 (155)
20	GNOMAD	ss4131532063	Apr 26, 2021 (155)
21	GNOMAD	ss4131532065	Apr 26, 2021 (155)
22	GNOMAD	ss4131532066	Apr 26, 2021 (155)
23	GNOMAD	ss4131532067	Apr 26, 2021 (155)
24	GNOMAD	ss4131532068	Apr 26, 2021 (155)
25	GNOMAD	ss4131532069	Apr 26, 2021 (155)
26	GNOMAD	ss4131532070	Apr 26, 2021 (155)
27	TOPMED	ss4683041866	Apr 26, 2021 (155)
28	TOPMED	ss4683041867	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5174699706	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5174699707	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5174699708	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5174699709	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5174699710	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5266273927	Oct 13, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5266273928	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5266273929	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5266273930	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5266273931	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5464194498	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5464194500	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5464194501	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5464194502	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5711940457	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5711940458	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5711940459	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5711940460	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5711940462	Oct 13, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996677 (NC_000005.10:149402689::A 8853/128030) Row 207996678 (NC_000005.10:149402689::AA 23123/127836) Row 207996679 (NC_000005.10:149402689::AAA 984/128046)...	-	Apr 26, 2021 (155)
62	Northern Sweden	NC_000005.9 - 148782253	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 32669013 (NC_000005.9:148782252::A 428/16742) Row 32669014 (NC_000005.9:148782252::AA 496/16742) Row 32669015 (NC_000005.9:148782252:AAAAAAAAA: 6/16742)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 32669013 (NC_000005.9:148782252::A 428/16742) Row 32669014 (NC_000005.9:148782252::AA 496/16742) Row 32669015 (NC_000005.9:148782252:AAAAAAAAA: 6/16742)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 32669013 (NC_000005.9:148782252::A 428/16742) Row 32669014 (NC_000005.9:148782252::AA 496/16742) Row 32669015 (NC_000005.9:148782252:AAAAAAAAA: 6/16742)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 32669013 (NC_000005.9:148782252::A 428/16742) Row 32669014 (NC_000005.9:148782252::AA 496/16742) Row 32669015 (NC_000005.9:148782252:AAAAAAAAA: 6/16742)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 32669013 (NC_000005.9:148782252::A 428/16742) Row 32669014 (NC_000005.9:148782252::AA 496/16742) Row 32669015 (NC_000005.9:148782252:AAAAAAAAA: 6/16742)...	-	Apr 26, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 45777561 (NC_000005.10:149402689::A 798/28256) Row 45777562 (NC_000005.10:149402689::AA 892/28256) Row 45777563 (NC_000005.10:149402689:A: 129/28256)...	-	Oct 13, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 45777561 (NC_000005.10:149402689::A 798/28256) Row 45777562 (NC_000005.10:149402689::AA 892/28256) Row 45777563 (NC_000005.10:149402689:A: 129/28256)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 45777561 (NC_000005.10:149402689::A 798/28256) Row 45777562 (NC_000005.10:149402689::AA 892/28256) Row 45777563 (NC_000005.10:149402689:A: 129/28256)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 45777561 (NC_000005.10:149402689::A 798/28256) Row 45777562 (NC_000005.10:149402689::AA 892/28256) Row 45777563 (NC_000005.10:149402689:A: 129/28256)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 45777561 (NC_000005.10:149402689::A 798/28256) Row 45777562 (NC_000005.10:149402689::AA 892/28256) Row 45777563 (NC_000005.10:149402689:A: 129/28256)...	-	Oct 13, 2022 (156)
73	TopMed Submission ignored due to conflicting rows: Row 520419423 (NC_000005.10:149402689:AAAAAA: 1/264690) Row 520419424 (NC_000005.10:149402689:AAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
74	TopMed Submission ignored due to conflicting rows: Row 520419423 (NC_000005.10:149402689:AAAAAA: 1/264690) Row 520419424 (NC_000005.10:149402689:AAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
75	ALFA	NC_000005.10 - 149402690	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4131532070	NC_000005.10:149402689:AAAAAAAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4131532069, ss4683041867	NC_000005.10:149402689:AAAAAAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss5174699708	NC_000005.9:148782252:AAAAAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5711940460	NC_000005.10:149402689:AAAAAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4131532068	NC_000005.10:149402689:AAAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4131532067, ss4683041866	NC_000005.10:149402689:AAAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4131532066, ss5266273931	NC_000005.10:149402689:AAAAA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3715937946, ss4131532065	NC_000005.10:149402689:AA:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3785281345, ss5174699709	NC_000005.9:148782252:A:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5266273930, ss5464194498, ss5711940459	NC_000005.10:149402689:A:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3715937945	NC_000005.10:149402690:A:	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss2997988610, ss5174699706	NC_000005.9:148782252::A	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4131532057, ss5266273928, ss5464194501, ss5711940457	NC_000005.10:149402689::A	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3715937944	NC_000005.10:149402691::A	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6204332, ss666332007, ss2997988609, ss3732919467, ss3829563321, ss3838255644, ss5174699707	NC_000005.9:148782252::AA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss947156181	NC_000005.9:148782253::AA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3843698691, ss4131532058, ss5266273927, ss5464194500, ss5711940458	NC_000005.10:149402689::AA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3715937943	NC_000005.10:149402691::AA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5174699710	NC_000005.9:148782252::AAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532059, ss5266273929, ss5464194502, ss5711940462	NC_000005.10:149402689::AAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532060	NC_000005.10:149402689::AAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532061	NC_000005.10:149402689::AAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532062	NC_000005.10:149402689::AAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9765777198	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532063	NC_000005.10:149402689::AAAAAAAA	NC_000005.10:149402689:AAAAAAAAAAA… NC_000005.10:149402689:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs370816490

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

rs370816490