Name: rs1307922193
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.

rs1307922193

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:154457968-154457984 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₅ / ins(T)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₄=0.00000 (0/11384, ALFA)
delTT=0.00000 (0/11384, ALFA)
delT=0.00000 (0/11384, ALFA) (+ 3 more)
dupT=0.00000 (0/11384, ALFA)
dupTTT=0.00000 (0/11384, ALFA)
delTT=0.129 (67/518, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IL6R : 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	11384	TTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7390	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2628	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	98	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2530	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	108	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	84	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	138	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	600	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	80	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	440	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=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	11384	(T)₁₇=1.00000	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	7390	(T)₁₇=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	2628	(T)₁₇=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	600	(T)₁₇=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	440	(T)₁₇=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(T)₁₇=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	108	(T)₁₇=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	80	(T)₁₇=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTTT=0.00
Northern Sweden	ACPOP	Study-wide	518	(T)₁₇=0.871	delTT=0.129

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.154457981_154457984del
GRCh38.p14 chr 1	NC_000001.11:g.154457982_154457984del
GRCh38.p14 chr 1	NC_000001.11:g.154457983_154457984del
GRCh38.p14 chr 1	NC_000001.11:g.154457984del
GRCh38.p14 chr 1	NC_000001.11:g.154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457983_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457982_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457981_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457979_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457974_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457973_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457970_154457984dup
GRCh38.p14 chr 1	NC_000001.11:g.154457984_154457985insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.154430457_154430460del
GRCh37.p13 chr 1	NC_000001.10:g.154430458_154430460del
GRCh37.p13 chr 1	NC_000001.10:g.154430459_154430460del
GRCh37.p13 chr 1	NC_000001.10:g.154430460del
GRCh37.p13 chr 1	NC_000001.10:g.154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430459_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430458_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430457_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430455_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430450_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430449_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430446_154430460dup
GRCh37.p13 chr 1	NC_000001.10:g.154430460_154430461insTTTTTTTTTTTTTTTTTT
IL6R RefSeqGene	NG_012087.1:g.57789_57792del
IL6R RefSeqGene	NG_012087.1:g.57790_57792del
IL6R RefSeqGene	NG_012087.1:g.57791_57792del
IL6R RefSeqGene	NG_012087.1:g.57792del
IL6R RefSeqGene	NG_012087.1:g.57792dup
IL6R RefSeqGene	NG_012087.1:g.57791_57792dup
IL6R RefSeqGene	NG_012087.1:g.57790_57792dup
IL6R RefSeqGene	NG_012087.1:g.57789_57792dup
IL6R RefSeqGene	NG_012087.1:g.57787_57792dup
IL6R RefSeqGene	NG_012087.1:g.57782_57792dup
IL6R RefSeqGene	NG_012087.1:g.57781_57792dup
IL6R RefSeqGene	NG_012087.1:g.57778_57792dup
IL6R RefSeqGene	NG_012087.1:g.57792_57793insTTTTTTTTTTTTTTTTTT

Gene: IL6R, interleukin 6 receptor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IL6R transcript variant 1	NM_000565.4:c.1160+3400_1… NM_000565.4:c.1160+3400_1160+3403del	N/A	Intron Variant
IL6R transcript variant 4	NM_001382769.1:c.1259+340… NM_001382769.1:c.1259+3400_1259+3403del	N/A	Intron Variant
IL6R transcript variant 5	NM_001382770.1:c.1253+340… NM_001382770.1:c.1253+3400_1253+3403del	N/A	Intron Variant
IL6R transcript variant 6	NM_001382771.1:c.1208+340… NM_001382771.1:c.1208+3400_1208+3403del	N/A	Intron Variant
IL6R transcript variant 7	NM_001382772.1:c.1154+340… NM_001382772.1:c.1154+3400_1154+3403del	N/A	Intron Variant
IL6R transcript variant 8	NM_001382773.1:c.1115-715… NM_001382773.1:c.1115-7153_1115-7150del	N/A	Intron Variant
IL6R transcript variant 9	NM_001382774.1:c.800+3400… NM_001382774.1:c.800+3400_800+3403del	N/A	Intron Variant
IL6R transcript variant 2	NM_181359.3:c.1067-7153_1… NM_181359.3:c.1067-7153_1067-7150del	N/A	Intron Variant
IL6R transcript variant 3	NM_001206866.2:c.	N/A	Genic Downstream Transcript Variant
IL6R transcript variant X8	XM_005245139.2:c.925-7153… XM_005245139.2:c.925-7153_925-7150del	N/A	Intron Variant
IL6R transcript variant X1	XM_017001199.2:c.1307+340… XM_017001199.2:c.1307+3400_1307+3403del	N/A	Intron Variant
IL6R transcript variant X2	XM_047419648.1:c.1244+340… XM_047419648.1:c.1244+3400_1244+3403del	N/A	Intron Variant
IL6R transcript variant X3	XM_047419649.1:c.1196+340… XM_047419649.1:c.1196+3400_1196+3403del	N/A	Intron Variant
IL6R transcript variant X4	XM_047419650.1:c.1097+340… XM_047419650.1:c.1097+3400_1097+3403del	N/A	Intron Variant
IL6R transcript variant X6	XM_047419655.1:c.973-7153… XM_047419655.1:c.973-7153_973-7150del	N/A	Intron Variant
IL6R transcript variant X5	XM_047419654.1:c.	N/A	Genic Downstream Transcript Variant
IL6R transcript variant X7	XM_047419656.1:c.	N/A	Genic Downstream Transcript Variant
IL6R transcript variant X9	XM_047419657.1:c.	N/A	Genic Downstream 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)₁₇=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆	dup(T)₁₁	dup(T)₁₂	dup(T)₁₅	ins(T)₁₈
GRCh38.p14 chr 1	NC_000001.11:g.154457968_154457984=	NC_000001.11:g.154457981_154457984del	NC_000001.11:g.154457982_154457984del	NC_000001.11:g.154457983_154457984del	NC_000001.11:g.154457984del	NC_000001.11:g.154457984dup	NC_000001.11:g.154457983_154457984dup	NC_000001.11:g.154457982_154457984dup	NC_000001.11:g.154457981_154457984dup	NC_000001.11:g.154457979_154457984dup	NC_000001.11:g.154457974_154457984dup	NC_000001.11:g.154457973_154457984dup	NC_000001.11:g.154457970_154457984dup	NC_000001.11:g.154457984_154457985insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.154430444_154430460=	NC_000001.10:g.154430457_154430460del	NC_000001.10:g.154430458_154430460del	NC_000001.10:g.154430459_154430460del	NC_000001.10:g.154430460del	NC_000001.10:g.154430460dup	NC_000001.10:g.154430459_154430460dup	NC_000001.10:g.154430458_154430460dup	NC_000001.10:g.154430457_154430460dup	NC_000001.10:g.154430455_154430460dup	NC_000001.10:g.154430450_154430460dup	NC_000001.10:g.154430449_154430460dup	NC_000001.10:g.154430446_154430460dup	NC_000001.10:g.154430460_154430461insTTTTTTTTTTTTTTTTTT
IL6R RefSeqGene	NG_012087.1:g.57776_57792=	NG_012087.1:g.57789_57792del	NG_012087.1:g.57790_57792del	NG_012087.1:g.57791_57792del	NG_012087.1:g.57792del	NG_012087.1:g.57792dup	NG_012087.1:g.57791_57792dup	NG_012087.1:g.57790_57792dup	NG_012087.1:g.57789_57792dup	NG_012087.1:g.57787_57792dup	NG_012087.1:g.57782_57792dup	NG_012087.1:g.57781_57792dup	NG_012087.1:g.57778_57792dup	NG_012087.1:g.57792_57793insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 1	NM_000565.3:c.1160+3387=	NM_000565.3:c.1160+3400_1160+3403del	NM_000565.3:c.1160+3401_1160+3403del	NM_000565.3:c.1160+3402_1160+3403del	NM_000565.3:c.1160+3403del	NM_000565.3:c.1160+3403dup	NM_000565.3:c.1160+3402_1160+3403dup	NM_000565.3:c.1160+3401_1160+3403dup	NM_000565.3:c.1160+3400_1160+3403dup	NM_000565.3:c.1160+3398_1160+3403dup	NM_000565.3:c.1160+3393_1160+3403dup	NM_000565.3:c.1160+3392_1160+3403dup	NM_000565.3:c.1160+3389_1160+3403dup	NM_000565.3:c.1160+3403_1160+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 1	NM_000565.4:c.1160+3387=	NM_000565.4:c.1160+3400_1160+3403del	NM_000565.4:c.1160+3401_1160+3403del	NM_000565.4:c.1160+3402_1160+3403del	NM_000565.4:c.1160+3403del	NM_000565.4:c.1160+3403dup	NM_000565.4:c.1160+3402_1160+3403dup	NM_000565.4:c.1160+3401_1160+3403dup	NM_000565.4:c.1160+3400_1160+3403dup	NM_000565.4:c.1160+3398_1160+3403dup	NM_000565.4:c.1160+3393_1160+3403dup	NM_000565.4:c.1160+3392_1160+3403dup	NM_000565.4:c.1160+3389_1160+3403dup	NM_000565.4:c.1160+3403_1160+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 4	NM_001382769.1:c.1259+3387=	NM_001382769.1:c.1259+3400_1259+3403del	NM_001382769.1:c.1259+3401_1259+3403del	NM_001382769.1:c.1259+3402_1259+3403del	NM_001382769.1:c.1259+3403del	NM_001382769.1:c.1259+3403dup	NM_001382769.1:c.1259+3402_1259+3403dup	NM_001382769.1:c.1259+3401_1259+3403dup	NM_001382769.1:c.1259+3400_1259+3403dup	NM_001382769.1:c.1259+3398_1259+3403dup	NM_001382769.1:c.1259+3393_1259+3403dup	NM_001382769.1:c.1259+3392_1259+3403dup	NM_001382769.1:c.1259+3389_1259+3403dup	NM_001382769.1:c.1259+3403_1259+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 5	NM_001382770.1:c.1253+3387=	NM_001382770.1:c.1253+3400_1253+3403del	NM_001382770.1:c.1253+3401_1253+3403del	NM_001382770.1:c.1253+3402_1253+3403del	NM_001382770.1:c.1253+3403del	NM_001382770.1:c.1253+3403dup	NM_001382770.1:c.1253+3402_1253+3403dup	NM_001382770.1:c.1253+3401_1253+3403dup	NM_001382770.1:c.1253+3400_1253+3403dup	NM_001382770.1:c.1253+3398_1253+3403dup	NM_001382770.1:c.1253+3393_1253+3403dup	NM_001382770.1:c.1253+3392_1253+3403dup	NM_001382770.1:c.1253+3389_1253+3403dup	NM_001382770.1:c.1253+3403_1253+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 6	NM_001382771.1:c.1208+3387=	NM_001382771.1:c.1208+3400_1208+3403del	NM_001382771.1:c.1208+3401_1208+3403del	NM_001382771.1:c.1208+3402_1208+3403del	NM_001382771.1:c.1208+3403del	NM_001382771.1:c.1208+3403dup	NM_001382771.1:c.1208+3402_1208+3403dup	NM_001382771.1:c.1208+3401_1208+3403dup	NM_001382771.1:c.1208+3400_1208+3403dup	NM_001382771.1:c.1208+3398_1208+3403dup	NM_001382771.1:c.1208+3393_1208+3403dup	NM_001382771.1:c.1208+3392_1208+3403dup	NM_001382771.1:c.1208+3389_1208+3403dup	NM_001382771.1:c.1208+3403_1208+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 7	NM_001382772.1:c.1154+3387=	NM_001382772.1:c.1154+3400_1154+3403del	NM_001382772.1:c.1154+3401_1154+3403del	NM_001382772.1:c.1154+3402_1154+3403del	NM_001382772.1:c.1154+3403del	NM_001382772.1:c.1154+3403dup	NM_001382772.1:c.1154+3402_1154+3403dup	NM_001382772.1:c.1154+3401_1154+3403dup	NM_001382772.1:c.1154+3400_1154+3403dup	NM_001382772.1:c.1154+3398_1154+3403dup	NM_001382772.1:c.1154+3393_1154+3403dup	NM_001382772.1:c.1154+3392_1154+3403dup	NM_001382772.1:c.1154+3389_1154+3403dup	NM_001382772.1:c.1154+3403_1154+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 8	NM_001382773.1:c.1115-7166=	NM_001382773.1:c.1115-7153_1115-7150del	NM_001382773.1:c.1115-7152_1115-7150del	NM_001382773.1:c.1115-7151_1115-7150del	NM_001382773.1:c.1115-7150del	NM_001382773.1:c.1115-7150dup	NM_001382773.1:c.1115-7151_1115-7150dup	NM_001382773.1:c.1115-7152_1115-7150dup	NM_001382773.1:c.1115-7153_1115-7150dup	NM_001382773.1:c.1115-7155_1115-7150dup	NM_001382773.1:c.1115-7160_1115-7150dup	NM_001382773.1:c.1115-7161_1115-7150dup	NM_001382773.1:c.1115-7164_1115-7150dup	NM_001382773.1:c.1115-7150_1115-7149insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 9	NM_001382774.1:c.800+3387=	NM_001382774.1:c.800+3400_800+3403del	NM_001382774.1:c.800+3401_800+3403del	NM_001382774.1:c.800+3402_800+3403del	NM_001382774.1:c.800+3403del	NM_001382774.1:c.800+3403dup	NM_001382774.1:c.800+3402_800+3403dup	NM_001382774.1:c.800+3401_800+3403dup	NM_001382774.1:c.800+3400_800+3403dup	NM_001382774.1:c.800+3398_800+3403dup	NM_001382774.1:c.800+3393_800+3403dup	NM_001382774.1:c.800+3392_800+3403dup	NM_001382774.1:c.800+3389_800+3403dup	NM_001382774.1:c.800+3403_800+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 2	NM_181359.2:c.1067-7166=	NM_181359.2:c.1067-7153_1067-7150del	NM_181359.2:c.1067-7152_1067-7150del	NM_181359.2:c.1067-7151_1067-7150del	NM_181359.2:c.1067-7150del	NM_181359.2:c.1067-7150dup	NM_181359.2:c.1067-7151_1067-7150dup	NM_181359.2:c.1067-7152_1067-7150dup	NM_181359.2:c.1067-7153_1067-7150dup	NM_181359.2:c.1067-7155_1067-7150dup	NM_181359.2:c.1067-7160_1067-7150dup	NM_181359.2:c.1067-7161_1067-7150dup	NM_181359.2:c.1067-7164_1067-7150dup	NM_181359.2:c.1067-7150_1067-7149insTTTTTTTTTTTTTTTTTT
IL6R transcript variant 2	NM_181359.3:c.1067-7166=	NM_181359.3:c.1067-7153_1067-7150del	NM_181359.3:c.1067-7152_1067-7150del	NM_181359.3:c.1067-7151_1067-7150del	NM_181359.3:c.1067-7150del	NM_181359.3:c.1067-7150dup	NM_181359.3:c.1067-7151_1067-7150dup	NM_181359.3:c.1067-7152_1067-7150dup	NM_181359.3:c.1067-7153_1067-7150dup	NM_181359.3:c.1067-7155_1067-7150dup	NM_181359.3:c.1067-7160_1067-7150dup	NM_181359.3:c.1067-7161_1067-7150dup	NM_181359.3:c.1067-7164_1067-7150dup	NM_181359.3:c.1067-7150_1067-7149insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X1	XM_005245138.1:c.1097+3387=	XM_005245138.1:c.1097+3400_1097+3403del	XM_005245138.1:c.1097+3401_1097+3403del	XM_005245138.1:c.1097+3402_1097+3403del	XM_005245138.1:c.1097+3403del	XM_005245138.1:c.1097+3403dup	XM_005245138.1:c.1097+3402_1097+3403dup	XM_005245138.1:c.1097+3401_1097+3403dup	XM_005245138.1:c.1097+3400_1097+3403dup	XM_005245138.1:c.1097+3398_1097+3403dup	XM_005245138.1:c.1097+3393_1097+3403dup	XM_005245138.1:c.1097+3392_1097+3403dup	XM_005245138.1:c.1097+3389_1097+3403dup	XM_005245138.1:c.1097+3403_1097+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X6	XM_005245139.1:c.925-7166=	XM_005245139.1:c.925-7153_925-7150del	XM_005245139.1:c.925-7152_925-7150del	XM_005245139.1:c.925-7151_925-7150del	XM_005245139.1:c.925-7150del	XM_005245139.1:c.925-7150dup	XM_005245139.1:c.925-7151_925-7150dup	XM_005245139.1:c.925-7152_925-7150dup	XM_005245139.1:c.925-7153_925-7150dup	XM_005245139.1:c.925-7155_925-7150dup	XM_005245139.1:c.925-7160_925-7150dup	XM_005245139.1:c.925-7161_925-7150dup	XM_005245139.1:c.925-7164_925-7150dup	XM_005245139.1:c.925-7150_925-7149insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X8	XM_005245139.2:c.925-7166=	XM_005245139.2:c.925-7153_925-7150del	XM_005245139.2:c.925-7152_925-7150del	XM_005245139.2:c.925-7151_925-7150del	XM_005245139.2:c.925-7150del	XM_005245139.2:c.925-7150dup	XM_005245139.2:c.925-7151_925-7150dup	XM_005245139.2:c.925-7152_925-7150dup	XM_005245139.2:c.925-7153_925-7150dup	XM_005245139.2:c.925-7155_925-7150dup	XM_005245139.2:c.925-7160_925-7150dup	XM_005245139.2:c.925-7161_925-7150dup	XM_005245139.2:c.925-7164_925-7150dup	XM_005245139.2:c.925-7150_925-7149insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X4	XM_005245140.1:c.*1+3387=	XM_005245140.1:c.1+3400_1+3403del	XM_005245140.1:c.1+3401_1+3403del	XM_005245140.1:c.1+3402_1+3403del	XM_005245140.1:c.*1+3403del	XM_005245140.1:c.*1+3403dup	XM_005245140.1:c.1+3402_1+3403dup	XM_005245140.1:c.1+3401_1+3403dup	XM_005245140.1:c.1+3400_1+3403dup	XM_005245140.1:c.1+3398_1+3403dup	XM_005245140.1:c.1+3393_1+3403dup	XM_005245140.1:c.1+3392_1+3403dup	XM_005245140.1:c.1+3389_1+3403dup	XM_005245140.1:c.1+3403_1+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X1	XM_017001199.2:c.1307+3387=	XM_017001199.2:c.1307+3400_1307+3403del	XM_017001199.2:c.1307+3401_1307+3403del	XM_017001199.2:c.1307+3402_1307+3403del	XM_017001199.2:c.1307+3403del	XM_017001199.2:c.1307+3403dup	XM_017001199.2:c.1307+3402_1307+3403dup	XM_017001199.2:c.1307+3401_1307+3403dup	XM_017001199.2:c.1307+3400_1307+3403dup	XM_017001199.2:c.1307+3398_1307+3403dup	XM_017001199.2:c.1307+3393_1307+3403dup	XM_017001199.2:c.1307+3392_1307+3403dup	XM_017001199.2:c.1307+3389_1307+3403dup	XM_017001199.2:c.1307+3403_1307+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X2	XM_047419648.1:c.1244+3387=	XM_047419648.1:c.1244+3400_1244+3403del	XM_047419648.1:c.1244+3401_1244+3403del	XM_047419648.1:c.1244+3402_1244+3403del	XM_047419648.1:c.1244+3403del	XM_047419648.1:c.1244+3403dup	XM_047419648.1:c.1244+3402_1244+3403dup	XM_047419648.1:c.1244+3401_1244+3403dup	XM_047419648.1:c.1244+3400_1244+3403dup	XM_047419648.1:c.1244+3398_1244+3403dup	XM_047419648.1:c.1244+3393_1244+3403dup	XM_047419648.1:c.1244+3392_1244+3403dup	XM_047419648.1:c.1244+3389_1244+3403dup	XM_047419648.1:c.1244+3403_1244+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X3	XM_047419649.1:c.1196+3387=	XM_047419649.1:c.1196+3400_1196+3403del	XM_047419649.1:c.1196+3401_1196+3403del	XM_047419649.1:c.1196+3402_1196+3403del	XM_047419649.1:c.1196+3403del	XM_047419649.1:c.1196+3403dup	XM_047419649.1:c.1196+3402_1196+3403dup	XM_047419649.1:c.1196+3401_1196+3403dup	XM_047419649.1:c.1196+3400_1196+3403dup	XM_047419649.1:c.1196+3398_1196+3403dup	XM_047419649.1:c.1196+3393_1196+3403dup	XM_047419649.1:c.1196+3392_1196+3403dup	XM_047419649.1:c.1196+3389_1196+3403dup	XM_047419649.1:c.1196+3403_1196+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X4	XM_047419650.1:c.1097+3387=	XM_047419650.1:c.1097+3400_1097+3403del	XM_047419650.1:c.1097+3401_1097+3403del	XM_047419650.1:c.1097+3402_1097+3403del	XM_047419650.1:c.1097+3403del	XM_047419650.1:c.1097+3403dup	XM_047419650.1:c.1097+3402_1097+3403dup	XM_047419650.1:c.1097+3401_1097+3403dup	XM_047419650.1:c.1097+3400_1097+3403dup	XM_047419650.1:c.1097+3398_1097+3403dup	XM_047419650.1:c.1097+3393_1097+3403dup	XM_047419650.1:c.1097+3392_1097+3403dup	XM_047419650.1:c.1097+3389_1097+3403dup	XM_047419650.1:c.1097+3403_1097+3404insTTTTTTTTTTTTTTTTTT
IL6R transcript variant X6	XM_047419655.1:c.973-7166=	XM_047419655.1:c.973-7153_973-7150del	XM_047419655.1:c.973-7152_973-7150del	XM_047419655.1:c.973-7151_973-7150del	XM_047419655.1:c.973-7150del	XM_047419655.1:c.973-7150dup	XM_047419655.1:c.973-7151_973-7150dup	XM_047419655.1:c.973-7152_973-7150dup	XM_047419655.1:c.973-7153_973-7150dup	XM_047419655.1:c.973-7155_973-7150dup	XM_047419655.1:c.973-7160_973-7150dup	XM_047419655.1:c.973-7161_973-7150dup	XM_047419655.1:c.973-7164_973-7150dup	XM_047419655.1:c.973-7150_973-7149insTTTTTTTTTTTTTTTTTT

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#.

38 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2987750844	Nov 08, 2017 (151)
2	MCHAISSO	ss3063609221	Jan 10, 2018 (151)
3	EVA_DECODE	ss3687780683	Jul 12, 2019 (153)
4	EVA_DECODE	ss3687780684	Jul 12, 2019 (153)
5	EVA_DECODE	ss3687780685	Jul 12, 2019 (153)
6	EVA_DECODE	ss3687780686	Jul 12, 2019 (153)
7	EVA_DECODE	ss3687780687	Jul 12, 2019 (153)
8	EVA_DECODE	ss3687780688	Jul 12, 2019 (153)
9	ACPOP	ss3727485074	Jul 12, 2019 (153)
10	EVA	ss3826423709	Apr 25, 2020 (154)
11	KOGIC	ss3945649330	Apr 25, 2020 (154)
12	KOGIC	ss3945649331	Apr 25, 2020 (154)
13	KOGIC	ss3945649332	Apr 25, 2020 (154)
14	GNOMAD	ss4003720162	Apr 25, 2021 (155)
15	GNOMAD	ss4003720163	Apr 25, 2021 (155)
16	GNOMAD	ss4003720164	Apr 25, 2021 (155)
17	GNOMAD	ss4003720165	Apr 25, 2021 (155)
18	GNOMAD	ss4003720169	Apr 25, 2021 (155)
19	GNOMAD	ss4003720170	Apr 25, 2021 (155)
20	GNOMAD	ss4003720171	Apr 25, 2021 (155)
21	GNOMAD	ss4003720172	Apr 25, 2021 (155)
22	GNOMAD	ss4003720174	Apr 25, 2021 (155)
23	GNOMAD	ss4003720175	Apr 25, 2021 (155)
24	GNOMAD	ss4003720176	Apr 25, 2021 (155)
25	GNOMAD	ss4003720177	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5146479102	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5146479103	Apr 25, 2021 (155)
28	TOMMO_GENOMICS	ss5146479104	Apr 25, 2021 (155)
29	HUGCELL_USP	ss5444884001	Oct 17, 2022 (156)
30	HUGCELL_USP	ss5444884002	Oct 17, 2022 (156)
31	HUGCELL_USP	ss5444884003	Oct 17, 2022 (156)
32	TOMMO_GENOMICS	ss5673673584	Oct 17, 2022 (156)
33	TOMMO_GENOMICS	ss5673673586	Oct 17, 2022 (156)
34	TOMMO_GENOMICS	ss5673673587	Oct 17, 2022 (156)
35	TOMMO_GENOMICS	ss5673673588	Oct 17, 2022 (156)
36	TOMMO_GENOMICS	ss5673673589	Oct 17, 2022 (156)
37	YY_MCH	ss5801259470	Oct 17, 2022 (156)
38	EVA	ss5849108583	Oct 17, 2022 (156)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 27026588 (NC_000001.11:154457967::T 126/85378) Row 27026589 (NC_000001.11:154457967::TT 3/85382) Row 27026590 (NC_000001.11:154457967::TTT 12/85376)...	-	Apr 25, 2021 (155)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 2027331 (NC_000001.11:154457968:TT: 203/1510) Row 2027332 (NC_000001.11:154457967:TTT: 7/1510) Row 2027333 (NC_000001.11:154457970::T 8/1510)	-	Apr 25, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 2027331 (NC_000001.11:154457968:TT: 203/1510) Row 2027332 (NC_000001.11:154457967:TTT: 7/1510) Row 2027333 (NC_000001.11:154457970::T 8/1510)	-	Apr 25, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 2027331 (NC_000001.11:154457968:TT: 203/1510) Row 2027332 (NC_000001.11:154457967:TTT: 7/1510) Row 2027333 (NC_000001.11:154457970::T 8/1510)	-	Apr 25, 2020 (154)
54	Northern Sweden	NC_000001.10 - 154430444	Jul 12, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 4448409 (NC_000001.10:154430443:TT: 1684/14252) Row 4448410 (NC_000001.10:154430443:T: 6/14252) Row 4448411 (NC_000001.10:154430443::TTT 7/14252)	-	Apr 25, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 4448409 (NC_000001.10:154430443:TT: 1684/14252) Row 4448410 (NC_000001.10:154430443:T: 6/14252) Row 4448411 (NC_000001.10:154430443::TTT 7/14252)	-	Apr 25, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 4448409 (NC_000001.10:154430443:TT: 1684/14252) Row 4448410 (NC_000001.10:154430443:T: 6/14252) Row 4448411 (NC_000001.10:154430443::TTT 7/14252)	-	Apr 25, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 7510688 (NC_000001.11:154457967:TT: 2185/24028) Row 7510690 (NC_000001.11:154457967::TTTTTTTTTTTTTTT 2/24028) Row 7510691 (NC_000001.11:154457967::TTT 12/24028)...	-	Oct 17, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 7510688 (NC_000001.11:154457967:TT: 2185/24028) Row 7510690 (NC_000001.11:154457967::TTTTTTTTTTTTTTT 2/24028) Row 7510691 (NC_000001.11:154457967::TTT 12/24028)...	-	Oct 17, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 7510688 (NC_000001.11:154457967:TT: 2185/24028) Row 7510690 (NC_000001.11:154457967::TTTTTTTTTTTTTTT 2/24028) Row 7510691 (NC_000001.11:154457967::TTT 12/24028)...	-	Oct 17, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 7510688 (NC_000001.11:154457967:TT: 2185/24028) Row 7510690 (NC_000001.11:154457967::TTTTTTTTTTTTTTT 2/24028) Row 7510691 (NC_000001.11:154457967::TTT 12/24028)...	-	Oct 17, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 7510688 (NC_000001.11:154457967:TT: 2185/24028) Row 7510690 (NC_000001.11:154457967::TTTTTTTTTTTTTTT 2/24028) Row 7510691 (NC_000001.11:154457967::TTT 12/24028)...	-	Oct 17, 2022 (156)
63	ALFA	NC_000001.11 - 154457968	Apr 25, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4003720177	NC_000001.11:154457967:TTTT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
612696663	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss2987750844	NC_000001.10:154430443:TTT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3687780683, ss3945649331, ss4003720176, ss5444884002, ss5673673588	NC_000001.11:154457967:TTT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
769939, ss3727485074, ss3826423709, ss5146479102	NC_000001.10:154430443:TT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3063609221, ss4003720175, ss5444884001, ss5673673584, ss5801259470, ss5849108583	NC_000001.11:154457967:TT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
612696663	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687780684, ss3945649330	NC_000001.11:154457968:TT:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5146479103	NC_000001.10:154430443:T:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4003720174, ss5444884003, ss5673673589	NC_000001.11:154457967:T:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
612696663	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3687780685	NC_000001.11:154457969:T:	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4003720162	NC_000001.11:154457967::T	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
612696663	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3687780686, ss3945649332	NC_000001.11:154457970::T	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4003720163	NC_000001.11:154457967::TT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3687780687	NC_000001.11:154457970::TT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5146479104	NC_000001.10:154430443::TTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4003720164, ss5673673587	NC_000001.11:154457967::TTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
612696663	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3687780688	NC_000001.11:154457970::TTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4003720165	NC_000001.11:154457967::TTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4003720169	NC_000001.11:154457967::TTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4003720170	NC_000001.11:154457967::TTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4003720171	NC_000001.11:154457967::TTTTTTTTTT… NC_000001.11:154457967::TTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5673673586	NC_000001.11:154457967::TTTTTTTTTT… NC_000001.11:154457967::TTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss4003720172	NC_000001.11:154457967::TTTTTTTTTT… NC_000001.11:154457967::TTTTTTTTTTTTTTTTTT	NC_000001.11:154457967:TTTTTTTTTTT… NC_000001.11:154457967:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1307922193

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1307922193