Name: rs34731685
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.

rs34731685

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:47319305-47319326 (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)₁₁ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.4042 (2024/5008, 1000G)
(T)₂₂=0.3179 (1423/4476, ALFA)
(T)₂₂=0.0062 (24/3854, ALSPAC) (+ 1 more)
(T)₂₂=0.0057 (21/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C5AR1 : 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	4476	TTTTTTTTTTTTTTTTTTTTTT=0.3179	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.6209, TTTTTTTTTTTTTTTTTTTTTTTT=0.0509, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0085, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018	0.347588	0.640477	0.011934	32
European	Sub	4436	TTTTTTTTTTTTTTTTTTTTTT=0.3131	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.6253, TTTTTTTTTTTTTTTTTTTTTTTT=0.0514, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0083, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018	0.342369	0.645582	0.012048	32
African	Sub	22	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	22	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	14	TTTTTTTTTTTTTTTTTTTTTT=0.57	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.36, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.07, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.666667	0.333333	0.0	4

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.4042
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.4372
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3899
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.4056
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.436
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.316
Allele Frequency Aggregator	Total	Global	4476	(T)₂₂=0.3179	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.6209, dupTT=0.0509, dupTTT=0.0085, dup(T)₆=0.0018
Allele Frequency Aggregator	European	Sub	4436	(T)₂₂=0.3131	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.6253, dupTT=0.0514, dupTTT=0.0083, dup(T)₆=0.0018
Allele Frequency Aggregator	African	Sub	22	(T)₂₂=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Other	Sub	14	(T)₂₂=0.57	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.36, dupTT=0.00, dupTTT=0.07, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₆=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₆=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₂=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₆=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₂=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₆=0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.9938
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.9943

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 19	NC_000019.10:g.47319316_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319317_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319318_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319319_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319320_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319321_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319323_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319324_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319325_47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319326del
GRCh38.p14 chr 19	NC_000019.10:g.47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319325_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319324_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319323_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319322_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319321_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319320_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319319_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319318_47319326dup
GRCh38.p14 chr 19	NC_000019.10:g.47319317_47319326dup
GRCh37.p13 chr 19	NC_000019.9:g.47822573_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822574_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822575_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822576_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822577_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822578_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822580_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822581_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822582_47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822583del
GRCh37.p13 chr 19	NC_000019.9:g.47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822582_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822581_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822580_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822579_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822578_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822577_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822576_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822575_47822583dup
GRCh37.p13 chr 19	NC_000019.9:g.47822574_47822583dup

Gene: C5AR1, complement C5a receptor 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C5AR1 transcript	NM_001736.4:c.4-465_4-455… NM_001736.4:c.4-465_4-455del	N/A	Intron Variant
C5AR1 transcript variant X1	XM_047439300.1:c.106-465_… XM_047439300.1:c.106-465_106-455del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₂=	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀
GRCh38.p14 chr 19	NC_000019.10:g.47319305_47319326=	NC_000019.10:g.47319316_47319326del	NC_000019.10:g.47319317_47319326del	NC_000019.10:g.47319318_47319326del	NC_000019.10:g.47319319_47319326del	NC_000019.10:g.47319320_47319326del	NC_000019.10:g.47319321_47319326del	NC_000019.10:g.47319323_47319326del	NC_000019.10:g.47319324_47319326del	NC_000019.10:g.47319325_47319326del	NC_000019.10:g.47319326del	NC_000019.10:g.47319326dup	NC_000019.10:g.47319325_47319326dup	NC_000019.10:g.47319324_47319326dup	NC_000019.10:g.47319323_47319326dup	NC_000019.10:g.47319322_47319326dup	NC_000019.10:g.47319321_47319326dup	NC_000019.10:g.47319320_47319326dup	NC_000019.10:g.47319319_47319326dup	NC_000019.10:g.47319318_47319326dup	NC_000019.10:g.47319317_47319326dup
GRCh37.p13 chr 19	NC_000019.9:g.47822562_47822583=	NC_000019.9:g.47822573_47822583del	NC_000019.9:g.47822574_47822583del	NC_000019.9:g.47822575_47822583del	NC_000019.9:g.47822576_47822583del	NC_000019.9:g.47822577_47822583del	NC_000019.9:g.47822578_47822583del	NC_000019.9:g.47822580_47822583del	NC_000019.9:g.47822581_47822583del	NC_000019.9:g.47822582_47822583del	NC_000019.9:g.47822583del	NC_000019.9:g.47822583dup	NC_000019.9:g.47822582_47822583dup	NC_000019.9:g.47822581_47822583dup	NC_000019.9:g.47822580_47822583dup	NC_000019.9:g.47822579_47822583dup	NC_000019.9:g.47822578_47822583dup	NC_000019.9:g.47822577_47822583dup	NC_000019.9:g.47822576_47822583dup	NC_000019.9:g.47822575_47822583dup	NC_000019.9:g.47822574_47822583dup
C5AR1 transcript	NM_001736.3:c.4-476=	NM_001736.3:c.4-465_4-455del	NM_001736.3:c.4-464_4-455del	NM_001736.3:c.4-463_4-455del	NM_001736.3:c.4-462_4-455del	NM_001736.3:c.4-461_4-455del	NM_001736.3:c.4-460_4-455del	NM_001736.3:c.4-458_4-455del	NM_001736.3:c.4-457_4-455del	NM_001736.3:c.4-456_4-455del	NM_001736.3:c.4-455del	NM_001736.3:c.4-455dup	NM_001736.3:c.4-456_4-455dup	NM_001736.3:c.4-457_4-455dup	NM_001736.3:c.4-458_4-455dup	NM_001736.3:c.4-459_4-455dup	NM_001736.3:c.4-460_4-455dup	NM_001736.3:c.4-461_4-455dup	NM_001736.3:c.4-462_4-455dup	NM_001736.3:c.4-463_4-455dup	NM_001736.3:c.4-464_4-455dup
C5AR1 transcript	NM_001736.4:c.4-476=	NM_001736.4:c.4-465_4-455del	NM_001736.4:c.4-464_4-455del	NM_001736.4:c.4-463_4-455del	NM_001736.4:c.4-462_4-455del	NM_001736.4:c.4-461_4-455del	NM_001736.4:c.4-460_4-455del	NM_001736.4:c.4-458_4-455del	NM_001736.4:c.4-457_4-455del	NM_001736.4:c.4-456_4-455del	NM_001736.4:c.4-455del	NM_001736.4:c.4-455dup	NM_001736.4:c.4-456_4-455dup	NM_001736.4:c.4-457_4-455dup	NM_001736.4:c.4-458_4-455dup	NM_001736.4:c.4-459_4-455dup	NM_001736.4:c.4-460_4-455dup	NM_001736.4:c.4-461_4-455dup	NM_001736.4:c.4-462_4-455dup	NM_001736.4:c.4-463_4-455dup	NM_001736.4:c.4-464_4-455dup
C5AR1 transcript variant X1	XM_005259190.1:c.-354-476=	XM_005259190.1:c.-354-465_-354-455del	XM_005259190.1:c.-354-464_-354-455del	XM_005259190.1:c.-354-463_-354-455del	XM_005259190.1:c.-354-462_-354-455del	XM_005259190.1:c.-354-461_-354-455del	XM_005259190.1:c.-354-460_-354-455del	XM_005259190.1:c.-354-458_-354-455del	XM_005259190.1:c.-354-457_-354-455del	XM_005259190.1:c.-354-456_-354-455del	XM_005259190.1:c.-354-455del	XM_005259190.1:c.-354-455dup	XM_005259190.1:c.-354-456_-354-455dup	XM_005259190.1:c.-354-457_-354-455dup	XM_005259190.1:c.-354-458_-354-455dup	XM_005259190.1:c.-354-459_-354-455dup	XM_005259190.1:c.-354-460_-354-455dup	XM_005259190.1:c.-354-461_-354-455dup	XM_005259190.1:c.-354-462_-354-455dup	XM_005259190.1:c.-354-463_-354-455dup	XM_005259190.1:c.-354-464_-354-455dup
C5AR1 transcript variant X1	XM_047439300.1:c.106-476=	XM_047439300.1:c.106-465_106-455del	XM_047439300.1:c.106-464_106-455del	XM_047439300.1:c.106-463_106-455del	XM_047439300.1:c.106-462_106-455del	XM_047439300.1:c.106-461_106-455del	XM_047439300.1:c.106-460_106-455del	XM_047439300.1:c.106-458_106-455del	XM_047439300.1:c.106-457_106-455del	XM_047439300.1:c.106-456_106-455del	XM_047439300.1:c.106-455del	XM_047439300.1:c.106-455dup	XM_047439300.1:c.106-456_106-455dup	XM_047439300.1:c.106-457_106-455dup	XM_047439300.1:c.106-458_106-455dup	XM_047439300.1:c.106-459_106-455dup	XM_047439300.1:c.106-460_106-455dup	XM_047439300.1:c.106-461_106-455dup	XM_047439300.1:c.106-462_106-455dup	XM_047439300.1:c.106-463_106-455dup	XM_047439300.1:c.106-464_106-455dup

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#.

50 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40989171	Mar 14, 2006 (126)
2	HGSV	ss77841897	Dec 07, 2007 (138)
3	HUMANGENOME_JCVI	ss95730402	Feb 04, 2009 (138)
4	PJP	ss294965234	May 09, 2011 (138)
5	SSMP	ss664447919	Apr 01, 2015 (144)
6	1000GENOMES	ss1378207464	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1709226769	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1709226790	Apr 01, 2015 (144)
9	SWEGEN	ss3017572707	Nov 08, 2017 (151)
10	EVA_DECODE	ss3702883938	Jul 13, 2019 (153)
11	EVA_DECODE	ss3702883939	Jul 13, 2019 (153)
12	EVA_DECODE	ss3702883940	Jul 13, 2019 (153)
13	EVA_DECODE	ss3702883941	Jul 13, 2019 (153)
14	KHV_HUMAN_GENOMES	ss3821380865	Jul 13, 2019 (153)
15	EVA	ss3835490562	Apr 27, 2020 (154)
16	GNOMAD	ss4332266051	Apr 27, 2021 (155)
17	GNOMAD	ss4332266052	Apr 27, 2021 (155)
18	GNOMAD	ss4332266053	Apr 27, 2021 (155)
19	GNOMAD	ss4332266054	Apr 27, 2021 (155)
20	GNOMAD	ss4332266055	Apr 27, 2021 (155)
21	GNOMAD	ss4332266056	Apr 27, 2021 (155)
22	GNOMAD	ss4332266057	Apr 27, 2021 (155)
23	GNOMAD	ss4332266058	Apr 27, 2021 (155)
24	GNOMAD	ss4332266059	Apr 27, 2021 (155)
25	GNOMAD	ss4332266060	Apr 27, 2021 (155)
26	GNOMAD	ss4332266062	Apr 27, 2021 (155)
27	GNOMAD	ss4332266063	Apr 27, 2021 (155)
28	GNOMAD	ss4332266064	Apr 27, 2021 (155)
29	GNOMAD	ss4332266065	Apr 27, 2021 (155)
30	GNOMAD	ss4332266066	Apr 27, 2021 (155)
31	GNOMAD	ss4332266067	Apr 27, 2021 (155)
32	GNOMAD	ss4332266068	Apr 27, 2021 (155)
33	GNOMAD	ss4332266069	Apr 27, 2021 (155)
34	GNOMAD	ss4332266070	Apr 27, 2021 (155)
35	GNOMAD	ss4332266071	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5228041522	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5228041523	Apr 27, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5307465134	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5307465135	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5307465136	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5499951299	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5499951300	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5499951301	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5786768940	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5786768941	Oct 13, 2022 (156)
46	YY_MCH	ss5817652722	Oct 13, 2022 (156)
47	EVA	ss5840632203	Oct 13, 2022 (156)
48	EVA	ss5840632204	Oct 13, 2022 (156)
49	EVA	ss5840632205	Oct 13, 2022 (156)
50	EVA	ss5953921046	Oct 13, 2022 (156)
51	1000Genomes	NC_000019.9 - 47822562	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 47822562	Oct 12, 2018 (152)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 541738740 (NC_000019.10:47319304::T 77844/87560) Row 541738741 (NC_000019.10:47319304::TT 5589/87402) Row 541738742 (NC_000019.10:47319304::TTT 262/87426)...	-	Apr 27, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 86010829 (NC_000019.9:47822561::T 12479/15210) Row 86010830 (NC_000019.9:47822561::TT 125/15210)	-	Apr 27, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 86010829 (NC_000019.9:47822561::T 12479/15210) Row 86010830 (NC_000019.9:47822561::TT 125/15210)	-	Apr 27, 2021 (155)
75	14KJPN Submission ignored due to conflicting rows: Row 120606044 (NC_000019.10:47319304::T 22483/26920) Row 120606045 (NC_000019.10:47319304::TT 191/26920)	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 120606044 (NC_000019.10:47319304::T 22483/26920) Row 120606045 (NC_000019.10:47319304::TT 191/26920)	-	Oct 13, 2022 (156)
77	UK 10K study - Twins	NC_000019.9 - 47822562	Oct 12, 2018 (152)
78	ALFA	NC_000019.10 - 47319305	Apr 27, 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)
rs56379598	May 15, 2013 (138)
rs72375121	May 11, 2012 (137)
rs148430073	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4332266071	NC_000019.10:47319304:TTTTTTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4332266070	NC_000019.10:47319304:TTTTTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4332266069	NC_000019.10:47319304:TTTTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3017572707	NC_000019.9:47822561:TTTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332266068	NC_000019.10:47319304:TTTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332266067	NC_000019.10:47319304:TTTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4332266066	NC_000019.10:47319304:TTTTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4332266065	NC_000019.10:47319304:TTTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4332266064	NC_000019.10:47319304:TTT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3702883938, ss4332266063	NC_000019.10:47319304:TT:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4332266062, ss5307465136, ss5499951301	NC_000019.10:47319304:T:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3702883939	NC_000019.10:47319305:T:	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss294965234	NC_000019.8:52514402::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
76814493, 42532509, 42532509, ss664447919, ss1378207464, ss1709226769, ss1709226790, ss3835490562, ss5228041522, ss5840632203, ss5953921046	NC_000019.9:47822561::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3821380865, ss4332266051, ss5307465134, ss5499951299, ss5786768940, ss5817652722	NC_000019.10:47319304::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702883940	NC_000019.10:47319306::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss40989171	NT_011109.16:20090779::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss77841897, ss95730402	NT_011109.16:20090801::T	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5228041523, ss5840632204	NC_000019.9:47822561::TT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266052, ss5307465135, ss5499951300, ss5786768941	NC_000019.10:47319304::TT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702883941	NC_000019.10:47319306::TT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5840632205	NC_000019.9:47822561::TTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
ss4332266053	NC_000019.10:47319304::TTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266054	NC_000019.10:47319304::TTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266055	NC_000019.10:47319304::TTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266056	NC_000019.10:47319304::TTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3009453485	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266057	NC_000019.10:47319304::TTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266058	NC_000019.10:47319304::TTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266059	NC_000019.10:47319304::TTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332266060	NC_000019.10:47319304::TTTTTTTTTT	NC_000019.10:47319304:TTTTTTTTTTTT… NC_000019.10:47319304:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34731685

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

rs34731685