Name: rs753687523
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.

rs753687523

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:4833458-4833478 (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)₇ / del(T)₆ / del…
del(T)₁₁ / del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₁=0.000004 (1/264690, TOPMED)
delT=0.1090 (869/7974, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TICAM1 : 2KB Upstream 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	7974	TTTTTTTTTTTTTTTTTTTTT=0.8824	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1090, TTTTTTTTTTTTTTTTTTTTTT=0.0079, TTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.809669	0.028244	0.162087	32
European	Sub	6704	TTTTTTTTTTTTTTTTTTTTT=0.8605	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1293, TTTTTTTTTTTTTTTTTTTTTT=0.0092, TTTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.773362	0.033677	0.192961	32
African	Sub	834	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	806	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	30	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	50	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	178	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	34	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	134	TTTTTTTTTTTTTTTTTTTTT=0.978	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.015, TTTTTTTTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.984848	0.0	0.015152	0

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
TopMed	Global	Study-wide	264690	(T)₂₁=0.999996	del(T)₁₁=0.000004
Allele Frequency Aggregator	Total	Global	7974	(T)₂₁=0.8824	del(T)₁₁=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.1090, dupT=0.0079, dupTT=0.0008, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	6704	(T)₂₁=0.8605	del(T)₁₁=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.1293, dupT=0.0092, dupTT=0.0009, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	834	(T)₂₁=1.000	del(T)₁₁=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	178	(T)₂₁=1.000	del(T)₁₁=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	134	(T)₂₁=0.978	del(T)₁₁=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTT=0.000, delT=0.015, dupT=0.007, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(T)₂₁=1.00	del(T)₁₁=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	40	(T)₂₁=1.00	del(T)₁₁=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(T)₂₁=1.00	del(T)₁₁=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

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.4833468_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833472_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833473_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833475_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833476_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833477_4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833478del
GRCh38.p14 chr 19	NC_000019.10:g.4833478dup
GRCh38.p14 chr 19	NC_000019.10:g.4833477_4833478dup
GRCh38.p14 chr 19	NC_000019.10:g.4833476_4833478dup
GRCh38.p14 chr 19	NC_000019.10:g.4833475_4833478dup
GRCh38.p14 chr 19	NC_000019.10:g.4833474_4833478dup
GRCh38.p14 chr 19	NC_000019.10:g.4833473_4833478dup
GRCh37.p13 chr 19	NC_000019.9:g.4833480_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833484_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833485_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833487_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833488_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833489_4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833490del
GRCh37.p13 chr 19	NC_000019.9:g.4833490dup
GRCh37.p13 chr 19	NC_000019.9:g.4833489_4833490dup
GRCh37.p13 chr 19	NC_000019.9:g.4833488_4833490dup
GRCh37.p13 chr 19	NC_000019.9:g.4833487_4833490dup
GRCh37.p13 chr 19	NC_000019.9:g.4833486_4833490dup
GRCh37.p13 chr 19	NC_000019.9:g.4833485_4833490dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3275_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3279_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3280_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3282_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3283_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3284_3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3285del
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3285dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3284_3285dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3283_3285dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3282_3285dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3281_3285dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3280_3285dup

Gene: TICAM1, toll like receptor adaptor molecule 1 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TICAM1 transcript variant 2	NM_001385678.1:c.	N/A	Upstream Transcript Variant
TICAM1 transcript variant 3	NM_001385679.1:c.	N/A	Upstream Transcript Variant
TICAM1 transcript variant 4	NM_001385680.1:c.	N/A	Upstream Transcript Variant
TICAM1 transcript variant 1	NM_182919.4:c.	N/A	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	(T)₂₁=	del(T)₁₁	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 19	NC_000019.10:g.4833458_4833478=	NC_000019.10:g.4833468_4833478del	NC_000019.10:g.4833472_4833478del	NC_000019.10:g.4833473_4833478del	NC_000019.10:g.4833475_4833478del	NC_000019.10:g.4833476_4833478del	NC_000019.10:g.4833477_4833478del	NC_000019.10:g.4833478del	NC_000019.10:g.4833478dup	NC_000019.10:g.4833477_4833478dup	NC_000019.10:g.4833476_4833478dup	NC_000019.10:g.4833475_4833478dup	NC_000019.10:g.4833474_4833478dup	NC_000019.10:g.4833473_4833478dup
GRCh37.p13 chr 19	NC_000019.9:g.4833470_4833490=	NC_000019.9:g.4833480_4833490del	NC_000019.9:g.4833484_4833490del	NC_000019.9:g.4833485_4833490del	NC_000019.9:g.4833487_4833490del	NC_000019.9:g.4833488_4833490del	NC_000019.9:g.4833489_4833490del	NC_000019.9:g.4833490del	NC_000019.9:g.4833490dup	NC_000019.9:g.4833489_4833490dup	NC_000019.9:g.4833488_4833490dup	NC_000019.9:g.4833487_4833490dup	NC_000019.9:g.4833486_4833490dup	NC_000019.9:g.4833485_4833490dup
TICAM1 RefSeqGene (LRG_358)	NG_031998.1:g.3265_3285=	NG_031998.1:g.3275_3285del	NG_031998.1:g.3279_3285del	NG_031998.1:g.3280_3285del	NG_031998.1:g.3282_3285del	NG_031998.1:g.3283_3285del	NG_031998.1:g.3284_3285del	NG_031998.1:g.3285del	NG_031998.1:g.3285dup	NG_031998.1:g.3284_3285dup	NG_031998.1:g.3283_3285dup	NG_031998.1:g.3282_3285dup	NG_031998.1:g.3281_3285dup	NG_031998.1:g.3280_3285dup

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#.

35 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss664448310	Apr 01, 2015 (144)
2	SWEGEN	ss3017011888	Nov 08, 2017 (151)
3	MCHAISSO	ss3065697587	Nov 08, 2017 (151)
4	PACBIO	ss3788453725	Jul 13, 2019 (153)
5	PACBIO	ss3793375977	Jul 13, 2019 (153)
6	PACBIO	ss3798262553	Jul 13, 2019 (153)
7	PACBIO	ss3798262554	Jul 13, 2019 (153)
8	EVA	ss3835325430	Apr 27, 2020 (154)
9	GNOMAD	ss4326852845	Apr 27, 2021 (155)
10	GNOMAD	ss4326852846	Apr 27, 2021 (155)
11	GNOMAD	ss4326852847	Apr 27, 2021 (155)
12	GNOMAD	ss4326852848	Apr 27, 2021 (155)
13	GNOMAD	ss4326852849	Apr 27, 2021 (155)
14	GNOMAD	ss4326852850	Apr 27, 2021 (155)
15	GNOMAD	ss4326852851	Apr 27, 2021 (155)
16	GNOMAD	ss4326852852	Apr 27, 2021 (155)
17	GNOMAD	ss4326852853	Apr 27, 2021 (155)
18	GNOMAD	ss4326852854	Apr 27, 2021 (155)
19	TOPMED	ss5066502416	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5226504066	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5226504067	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5226504068	Apr 27, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5306320258	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5306320259	Oct 16, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5306320260	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5306320261	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5306320262	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5498973046	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5498973047	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5498973048	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5498973049	Oct 16, 2022 (156)
32	SANFORD_IMAGENETICS	ss5661881995	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5784702415	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5784702416	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5784702417	Oct 16, 2022 (156)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532747827 (NC_000019.10:4833457::T 2474/96254) Row 532747828 (NC_000019.10:4833457::TT 92/96252) Row 532747829 (NC_000019.10:4833457::TTT 14/96252)...	-	Apr 27, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 84473373 (NC_000019.9:4833469:T: 5990/16546) Row 84473374 (NC_000019.9:4833469:TT: 18/16546) Row 84473375 (NC_000019.9:4833469::T 35/16546)	-	Apr 27, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 84473373 (NC_000019.9:4833469:T: 5990/16546) Row 84473374 (NC_000019.9:4833469:TT: 18/16546) Row 84473375 (NC_000019.9:4833469::T 35/16546)	-	Apr 27, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 84473373 (NC_000019.9:4833469:T: 5990/16546) Row 84473374 (NC_000019.9:4833469:TT: 18/16546) Row 84473375 (NC_000019.9:4833469::T 35/16546)	-	Apr 27, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 118539519 (NC_000019.10:4833457:T: 11221/28166) Row 118539520 (NC_000019.10:4833457:TT: 32/28166) Row 118539521 (NC_000019.10:4833457::T 48/28166)	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 118539519 (NC_000019.10:4833457:T: 11221/28166) Row 118539520 (NC_000019.10:4833457:TT: 32/28166) Row 118539521 (NC_000019.10:4833457::T 48/28166)	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 118539519 (NC_000019.10:4833457:T: 11221/28166) Row 118539520 (NC_000019.10:4833457:TT: 32/28166) Row 118539521 (NC_000019.10:4833457::T 48/28166)	-	Oct 16, 2022 (156)
53	TopMed	NC_000019.10 - 4833458	Apr 27, 2021 (155)
54	ALFA	NC_000019.10 - 4833458	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
282048080, ss5066502416	NC_000019.10:4833457:TTTTTTTTTTT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4326852854	NC_000019.10:4833457:TTTTTT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4326852853	NC_000019.10:4833457:TTTT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4326852852, ss5498973049	NC_000019.10:4833457:TTT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3017011888, ss3788453725, ss3798262553, ss5226504067	NC_000019.9:4833469:TT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4326852851, ss5306320260, ss5498973048, ss5784702416	NC_000019.10:4833457:TT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3793375977, ss3798262554, ss3835325430, ss5226504066, ss5661881995	NC_000019.9:4833469:T:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3065697587, ss5306320258, ss5498973046, ss5784702415	NC_000019.10:4833457:T:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss664448310, ss5226504068	NC_000019.9:4833469::T	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852845, ss5306320259, ss5498973047, ss5784702417	NC_000019.10:4833457::T	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852846, ss5306320261	NC_000019.10:4833457::TT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852847, ss5306320262	NC_000019.10:4833457::TTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
2731687771	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852848	NC_000019.10:4833457::TTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852849	NC_000019.10:4833457::TTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326852850	NC_000019.10:4833457::TTTTTT	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3286683784	NC_000019.10:4833457:TTTTTTT:	NC_000019.10:4833457:TTTTTTTTTTTTT… NC_000019.10:4833457:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs753687523

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

rs753687523