Name: rs74750424
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.

rs74750424

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:6709523-6709539 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / 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: del(T)₅=0.3794 (1900/5008, 1000G)
dupT=0.3462 (1639/4734, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GRM7-AS3 : Intron Variant
LOC105376944 : 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	4734	TTTTTTTTTTTTTTTTT=0.3492	TTTTTTTTTTT=0.0027, TTTTTTTTTTTT=0.2847, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0112, TTTTTTTTTTTTTTTTTT=0.3462, TTTTTTTTTTTTTTTTTTT=0.0044, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.39153	0.375108	0.233362	32
European	Sub	4566	TTTTTTTTTTTTTTTTT=0.3270	TTTTTTTTTTT=0.0028, TTTTTTTTTTTT=0.2946, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0112, TTTTTTTTTTTTTTTTTT=0.3583, TTTTTTTTTTTTTTTTTTT=0.0046, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.346654	0.402416	0.250929	32
African	Sub	120	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	114	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	22	TTTTTTTTTTTTTTTTT=0.64	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.14, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTT=0.14, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	0.875	0.125	0.0	5

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₁₇=0.6206	del(T)₅=0.3794
1000Genomes	African	Sub	1322	(T)₁₇=0.5371	del(T)₅=0.4629
1000Genomes	East Asian	Sub	1008	(T)₁₇=0.7411	del(T)₅=0.2589
1000Genomes	Europe	Sub	1006	(T)₁₇=0.5507	del(T)₅=0.4493
1000Genomes	South Asian	Sub	978	(T)₁₇=0.777	del(T)₅=0.223
1000Genomes	American	Sub	694	(T)₁₇=0.486	del(T)₅=0.514
Allele Frequency Aggregator	Total	Global	4734	(T)₁₇=0.3492	del(T)₆=0.0027, del(T)₅=0.2847, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0112, dupT=0.3462, dupTT=0.0044, dupTTT=0.0000, dup(T)₅=0.0000, dup(T)₉=0.0015
Allele Frequency Aggregator	European	Sub	4566	(T)₁₇=0.3270	del(T)₆=0.0028, del(T)₅=0.2946, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0112, dupT=0.3583, dupTT=0.0046, dupTTT=0.0000, dup(T)₅=0.0000, dup(T)₉=0.0015
Allele Frequency Aggregator	African	Sub	120	(T)₁₇=1.000	del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000, dup(T)₉=0.000
Allele Frequency Aggregator	Other	Sub	22	(T)₁₇=0.64	del(T)₆=0.00, del(T)₅=0.14, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.09, dupT=0.14, dupTT=0.00, dupTTT=0.00, dup(T)₅=0.00, dup(T)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(T)₁₇=1.0	del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₉=0.0
Allele Frequency Aggregator	Latin American 1	Sub	8	(T)₁₇=1.0	del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₉=0.0
Allele Frequency Aggregator	Latin American 2	Sub	4	(T)₁₇=1.0	del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₉=0.0
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₇=1.0	del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₉=0.0

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.6709534_6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709535_6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709536_6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709537_6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709538_6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709539del
GRCh38.p14 chr 3	NC_000003.12:g.6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709538_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709537_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709536_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709535_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709534_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709533_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709532_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709531_6709539dup
GRCh38.p14 chr 3	NC_000003.12:g.6709530_6709539dup
GRCh37.p13 chr 3	NC_000003.11:g.6751221_6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751222_6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751223_6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751224_6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751225_6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751226del
GRCh37.p13 chr 3	NC_000003.11:g.6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751225_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751224_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751223_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751222_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751221_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751220_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751219_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751218_6751226dup
GRCh37.p13 chr 3	NC_000003.11:g.6751217_6751226dup

Gene: GRM7-AS3, GRM7 antisense RNA 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GRM7-AS3 transcript variant 1	NR_110123.1:n.	N/A	Intron Variant
GRM7-AS3 transcript variant 2	NR_110125.1:n.	N/A	Genic Downstream Transcript Variant

Gene: LOC105376944, uncharacterized LOC105376944 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105376944 transcript variant X5	XR_001740417.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X10	XR_001740418.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X2	XR_002959674.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X1	XR_007095802.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X3	XR_007095803.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X4	XR_007095804.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X6	XR_007095805.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X7	XR_007095806.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X8	XR_007095807.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X9	XR_007095808.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X11	XR_007095809.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X12	XR_007095810.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X13	XR_007095811.1:n.	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)₁₇=	del(T)₆	del(T)₅	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 3	NC_000003.12:g.6709523_6709539=	NC_000003.12:g.6709534_6709539del	NC_000003.12:g.6709535_6709539del	NC_000003.12:g.6709536_6709539del	NC_000003.12:g.6709537_6709539del	NC_000003.12:g.6709538_6709539del	NC_000003.12:g.6709539del	NC_000003.12:g.6709539dup	NC_000003.12:g.6709538_6709539dup	NC_000003.12:g.6709537_6709539dup	NC_000003.12:g.6709536_6709539dup	NC_000003.12:g.6709535_6709539dup	NC_000003.12:g.6709534_6709539dup	NC_000003.12:g.6709533_6709539dup	NC_000003.12:g.6709532_6709539dup	NC_000003.12:g.6709531_6709539dup	NC_000003.12:g.6709530_6709539dup
GRCh37.p13 chr 3	NC_000003.11:g.6751210_6751226=	NC_000003.11:g.6751221_6751226del	NC_000003.11:g.6751222_6751226del	NC_000003.11:g.6751223_6751226del	NC_000003.11:g.6751224_6751226del	NC_000003.11:g.6751225_6751226del	NC_000003.11:g.6751226del	NC_000003.11:g.6751226dup	NC_000003.11:g.6751225_6751226dup	NC_000003.11:g.6751224_6751226dup	NC_000003.11:g.6751223_6751226dup	NC_000003.11:g.6751222_6751226dup	NC_000003.11:g.6751221_6751226dup	NC_000003.11:g.6751220_6751226dup	NC_000003.11:g.6751219_6751226dup	NC_000003.11:g.6751218_6751226dup	NC_000003.11:g.6751217_6751226dup

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#.

82 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77841337	Apr 25, 2013 (138)
2	BCMHGSC_JDW	ss103663120	Dec 01, 2009 (131)
3	GMI	ss288319476	May 04, 2012 (137)
4	GMI	ss288319478	May 31, 2013 (142)
5	PJP	ss295086497	May 31, 2013 (138)
6	PJP	ss295086498	May 09, 2011 (134)
7	BILGI_BIOE	ss666195974	Apr 25, 2013 (138)
8	SSIP	ss947079790	Aug 21, 2014 (142)
9	1000GENOMES	ss1369923751	Aug 21, 2014 (142)
10	EVA_UK10K_ALSPAC	ss1703499566	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1703499600	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710065651	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710065657	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1798795223	Sep 08, 2015 (146)
15	SYSTEMSBIOZJU	ss2625147587	Nov 08, 2017 (151)
16	SWEGEN	ss2991771597	Nov 08, 2017 (151)
17	MCHAISSO	ss3065865227	Nov 08, 2017 (151)
18	BEROUKHIMLAB	ss3644118951	Oct 11, 2018 (152)
19	EVA_DECODE	ss3708564980	Jul 13, 2019 (153)
20	EVA_DECODE	ss3708564981	Jul 13, 2019 (153)
21	EVA_DECODE	ss3708564982	Jul 13, 2019 (153)
22	EVA_DECODE	ss3708564983	Jul 13, 2019 (153)
23	EVA_DECODE	ss3708564984	Jul 13, 2019 (153)
24	EVA_DECODE	ss3708564985	Jul 13, 2019 (153)
25	ACPOP	ss3729600001	Jul 13, 2019 (153)
26	ACPOP	ss3729600002	Jul 13, 2019 (153)
27	ACPOP	ss3729600003	Jul 13, 2019 (153)
28	PACBIO	ss3784224656	Jul 13, 2019 (153)
29	PACBIO	ss3789754698	Jul 13, 2019 (153)
30	PACBIO	ss3789754699	Jul 13, 2019 (153)
31	PACBIO	ss3794628425	Jul 13, 2019 (153)
32	PACBIO	ss3794628426	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3802765812	Jul 13, 2019 (153)
34	EVA	ss3827642043	Apr 25, 2020 (154)
35	KOGIC	ss3950592689	Apr 25, 2020 (154)
36	KOGIC	ss3950592690	Apr 25, 2020 (154)
37	KOGIC	ss3950592691	Apr 25, 2020 (154)
38	KOGIC	ss3950592692	Apr 25, 2020 (154)
39	KOGIC	ss3950592693	Apr 25, 2020 (154)
40	GNOMAD	ss4065256023	Apr 26, 2021 (155)
41	GNOMAD	ss4065256024	Apr 26, 2021 (155)
42	GNOMAD	ss4065256025	Apr 26, 2021 (155)
43	GNOMAD	ss4065256026	Apr 26, 2021 (155)
44	GNOMAD	ss4065256027	Apr 26, 2021 (155)
45	GNOMAD	ss4065256028	Apr 26, 2021 (155)
46	GNOMAD	ss4065256029	Apr 26, 2021 (155)
47	GNOMAD	ss4065256030	Apr 26, 2021 (155)
48	GNOMAD	ss4065256031	Apr 26, 2021 (155)
49	GNOMAD	ss4065256032	Apr 26, 2021 (155)
50	GNOMAD	ss4065256034	Apr 26, 2021 (155)
51	GNOMAD	ss4065256035	Apr 26, 2021 (155)
52	GNOMAD	ss4065256036	Apr 26, 2021 (155)
53	GNOMAD	ss4065256037	Apr 26, 2021 (155)
54	GNOMAD	ss4065256038	Apr 26, 2021 (155)
55	GNOMAD	ss4065256039	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5157637276	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5157637277	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5157637278	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5157637279	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5157637280	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5157637281	Apr 26, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5252921843	Oct 12, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5252921844	Oct 12, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5252921845	Oct 12, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5252921846	Oct 12, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5252921847	Oct 12, 2022 (156)
67	1000G_HIGH_COVERAGE	ss5252921848	Oct 12, 2022 (156)
68	HUGCELL_USP	ss5452437192	Oct 12, 2022 (156)
69	HUGCELL_USP	ss5452437193	Oct 12, 2022 (156)
70	HUGCELL_USP	ss5452437194	Oct 12, 2022 (156)
71	HUGCELL_USP	ss5452437195	Oct 12, 2022 (156)
72	HUGCELL_USP	ss5452437196	Oct 12, 2022 (156)
73	HUGCELL_USP	ss5452437197	Oct 12, 2022 (156)
74	TOMMO_GENOMICS	ss5688858867	Oct 12, 2022 (156)
75	TOMMO_GENOMICS	ss5688858868	Oct 12, 2022 (156)
76	TOMMO_GENOMICS	ss5688858869	Oct 12, 2022 (156)
77	TOMMO_GENOMICS	ss5688858870	Oct 12, 2022 (156)
78	TOMMO_GENOMICS	ss5688858871	Oct 12, 2022 (156)
79	TOMMO_GENOMICS	ss5688858872	Oct 12, 2022 (156)
80	EVA	ss5825296224	Oct 12, 2022 (156)
81	EVA	ss5825296225	Oct 12, 2022 (156)
82	EVA	ss5867483181	Oct 12, 2022 (156)
83	1000Genomes	NC_000003.11 - 6751210	Oct 11, 2018 (152)
84	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7645871 (NC_000003.11:6751210:TTTT: 2815/3854) Row 7645872 (NC_000003.11:6751209:TTTTTT: 108/3854)	-	Oct 11, 2018 (152)
85	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7645871 (NC_000003.11:6751210:TTTT: 2815/3854) Row 7645872 (NC_000003.11:6751209:TTTTTT: 108/3854)	-	Oct 11, 2018 (152)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98021803 (NC_000003.12:6709522::T 46402/122898) Row 98021804 (NC_000003.12:6709522::TT 1045/124150) Row 98021805 (NC_000003.12:6709522::TTT 3/124232)...	-	Apr 26, 2021 (155)
102	Korean Genome Project Submission ignored due to conflicting rows: Row 6970690 (NC_000003.12:6709525:TT: 27/1832) Row 6970691 (NC_000003.12:6709526:T: 409/1832) Row 6970692 (NC_000003.12:6709527::T 696/1832)...	-	Apr 25, 2020 (154)
103	Korean Genome Project Submission ignored due to conflicting rows: Row 6970690 (NC_000003.12:6709525:TT: 27/1832) Row 6970691 (NC_000003.12:6709526:T: 409/1832) Row 6970692 (NC_000003.12:6709527::T 696/1832)...	-	Apr 25, 2020 (154)
104	Korean Genome Project Submission ignored due to conflicting rows: Row 6970690 (NC_000003.12:6709525:TT: 27/1832) Row 6970691 (NC_000003.12:6709526:T: 409/1832) Row 6970692 (NC_000003.12:6709527::T 696/1832)...	-	Apr 25, 2020 (154)
105	Korean Genome Project Submission ignored due to conflicting rows: Row 6970690 (NC_000003.12:6709525:TT: 27/1832) Row 6970691 (NC_000003.12:6709526:T: 409/1832) Row 6970692 (NC_000003.12:6709527::T 696/1832)...	-	Apr 25, 2020 (154)
106	Korean Genome Project Submission ignored due to conflicting rows: Row 6970690 (NC_000003.12:6709525:TT: 27/1832) Row 6970691 (NC_000003.12:6709526:T: 409/1832) Row 6970692 (NC_000003.12:6709527::T 696/1832)...	-	Apr 25, 2020 (154)
107	Northern Sweden Submission ignored due to conflicting rows: Row 2884866 (NC_000003.11:6751209:TTTTT: 215/586) Row 2884867 (NC_000003.11:6751209::T 108/586) Row 2884868 (NC_000003.11:6751209::TTTTTTTTT 8/586)	-	Jul 13, 2019 (153)
108	Northern Sweden Submission ignored due to conflicting rows: Row 2884866 (NC_000003.11:6751209:TTTTT: 215/586) Row 2884867 (NC_000003.11:6751209::T 108/586) Row 2884868 (NC_000003.11:6751209::TTTTTTTTT 8/586)	-	Jul 13, 2019 (153)
109	Northern Sweden Submission ignored due to conflicting rows: Row 2884866 (NC_000003.11:6751209:TTTTT: 215/586) Row 2884867 (NC_000003.11:6751209::T 108/586) Row 2884868 (NC_000003.11:6751209::TTTTTTTTT 8/586)	-	Jul 13, 2019 (153)
110	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
112	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
114	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
115	8.3KJPN Submission ignored due to conflicting rows: Row 15606583 (NC_000003.11:6751209::T 8709/16760) Row 15606584 (NC_000003.11:6751209:T: 3426/16760) Row 15606585 (NC_000003.11:6751209::TT 193/16760)...	-	Apr 26, 2021 (155)
116	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
117	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
118	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
120	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
121	14KJPN Submission ignored due to conflicting rows: Row 22695971 (NC_000003.12:6709522:T: 5725/28254) Row 22695972 (NC_000003.12:6709522::T 14769/28254) Row 22695973 (NC_000003.12:6709522:TTTTT: 3239/28254)...	-	Oct 12, 2022 (156)
122	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7645871 (NC_000003.11:6751210:TTTT: 2655/3708) Row 7645872 (NC_000003.11:6751209:TTTTTT: 120/3708)	-	Oct 11, 2018 (152)
123	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7645871 (NC_000003.11:6751210:TTTT: 2655/3708) Row 7645872 (NC_000003.11:6751209:TTTTTT: 120/3708)	-	Oct 11, 2018 (152)
124	ALFA	NC_000003.12 - 6709523	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs386355737	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1703499566, ss1703499600, ss2991771597, ss5157637281, ss5825296225	NC_000003.11:6751209:TTTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3708564980, ss4065256039, ss5452437196, ss5688858872	NC_000003.12:6709522:TTTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss103663120	NT_022517.18:6691220:TTTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss295086498	NC_000003.10:6726221:TTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
13796263, ss1369923751, ss1798795223, ss3644118951, ss3729600001, ss3784224656, ss3789754698, ss3794628425, ss3827642043, ss5157637279, ss5825296224	NC_000003.11:6751209:TTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1710065651, ss1710065657	NC_000003.11:6751210:TTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3802765812, ss3950592693, ss4065256038, ss5252921843, ss5452437192, ss5688858869, ss5867483181	NC_000003.12:6709522:TTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3708564981	NC_000003.12:6709523:TTTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
	NC_000003.11:6751210:TTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4065256037, ss5252921846, ss5452437195	NC_000003.12:6709522:TTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3708564982	NC_000003.12:6709524:TTTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4065256036	NC_000003.12:6709522:TTT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5157637280	NC_000003.11:6751209:TT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4065256035, ss5252921848, ss5688858871	NC_000003.12:6709522:TT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3950592689	NC_000003.12:6709525:TT:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss288319476	NC_000003.10:6726209:T:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss2625147587, ss5157637277	NC_000003.11:6751209:T:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3065865227, ss4065256034, ss5252921844, ss5452437197, ss5688858867	NC_000003.12:6709522:T:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3950592690	NC_000003.12:6709526:T:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3708564983	NC_000003.12:6709527:T:	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295086497	NC_000003.10:6726210::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss288319478	NC_000003.10:6726226::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss666195974, ss3729600002, ss3789754699, ss3794628426, ss5157637276	NC_000003.11:6751209::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss947079790	NC_000003.11:6751214::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4065256023, ss5252921845, ss5452437193, ss5688858868	NC_000003.12:6709522::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3950592691	NC_000003.12:6709527::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3708564984	NC_000003.12:6709528::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss77841337	NT_022517.18:6691226::T	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5157637278	NC_000003.11:6751209::TT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4065256024, ss5252921847, ss5452437194, ss5688858870	NC_000003.12:6709522::TT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3950592692	NC_000003.12:6709527::TT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3708564985	NC_000003.12:6709528::TT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4065256025	NC_000003.12:6709522::TTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4065256026	NC_000003.12:6709522::TTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256027	NC_000003.12:6709522::TTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256028	NC_000003.12:6709522::TTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256029	NC_000003.12:6709522::TTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256030	NC_000003.12:6709522::TTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3729600003	NC_000003.11:6751209::TTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256031	NC_000003.12:6709522::TTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7373697855	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065256032	NC_000003.12:6709522::TTTTTTTTTT	NC_000003.12:6709522:TTTTTTTTTTTTT… NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs74750424

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

rs74750424