Name: rs34630774
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.

rs34630774

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:149261625-149261640 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₆ / del(A)₅ / delAAA / delAA…
del(A)₆ / del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₆=0.0000 (0/2570, ALFA)
del(A)₅=0.0000 (0/2570, ALFA)
delAAA=0.0000 (0/2570, ALFA) (+ 5 more)
delAA=0.0000 (0/2570, ALFA)
delA=0.0000 (0/2570, ALFA)
dupA=0.0000 (0/2570, ALFA)
(A)₁₆=0.456 (258/566, NorthernSweden)
(A)₁₆=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF783 : 2KB Upstream Variant
LOC124901769 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	2570	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1896	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	432	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	416	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	46	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	30	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	16	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	86	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	74	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	2570	(A)₁₆=1.0000	del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	European	Sub	1896	(A)₁₆=1.0000	del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	African	Sub	432	(A)₁₆=1.000	del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	86	(A)₁₆=1.00	del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Other	Sub	74	(A)₁₆=1.00	del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Asian	Sub	46	(A)₁₆=1.00	del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₁₆=1.00	del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(A)₁₆=1.00	del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Northern Sweden	ACPOP	Study-wide	566	(A)₁₆=0.456	delAA=0.544
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₆=0.47	delAA=0.53

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 7	NC_000007.14:g.149261635_149261640del
GRCh38.p14 chr 7	NC_000007.14:g.149261636_149261640del
GRCh38.p14 chr 7	NC_000007.14:g.149261638_149261640del
GRCh38.p14 chr 7	NC_000007.14:g.149261639_149261640del
GRCh38.p14 chr 7	NC_000007.14:g.149261640del
GRCh38.p14 chr 7	NC_000007.14:g.149261640dup
GRCh38.p14 chr 7	NC_000007.14:g.149261639_149261640dup
GRCh38.p14 chr 7	NC_000007.14:g.149261638_149261640dup
GRCh37.p13 chr 7	NC_000007.13:g.148958726_148958731del
GRCh37.p13 chr 7	NC_000007.13:g.148958727_148958731del
GRCh37.p13 chr 7	NC_000007.13:g.148958729_148958731del
GRCh37.p13 chr 7	NC_000007.13:g.148958730_148958731del
GRCh37.p13 chr 7	NC_000007.13:g.148958731del
GRCh37.p13 chr 7	NC_000007.13:g.148958731dup
GRCh37.p13 chr 7	NC_000007.13:g.148958730_148958731dup
GRCh37.p13 chr 7	NC_000007.13:g.148958729_148958731dup

Gene: ZNF783, zinc finger protein 783 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF783 transcript variant 1	NM_001195220.2:c.	N/A	Upstream Transcript Variant
ZNF783 transcript variant 2	NR_144366.2:n.	N/A	Upstream Transcript Variant
ZNF783 transcript variant 3	NR_144367.1:n.	N/A	N/A
ZNF783 transcript variant X2	XM_047419692.1:c.	N/A	Upstream Transcript Variant
ZNF783 transcript variant X1	XM_011515701.3:c.	N/A	N/A
ZNF783 transcript variant X3	XR_001744503.2:n.	N/A	N/A

Gene: LOC124901769, uncharacterized LOC124901769 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124901769 transcript	XR_007060582.1: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	(A)₁₆=	del(A)₆	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 7	NC_000007.14:g.149261625_149261640=	NC_000007.14:g.149261635_149261640del	NC_000007.14:g.149261636_149261640del	NC_000007.14:g.149261638_149261640del	NC_000007.14:g.149261639_149261640del	NC_000007.14:g.149261640del	NC_000007.14:g.149261640dup	NC_000007.14:g.149261639_149261640dup	NC_000007.14:g.149261638_149261640dup
GRCh37.p13 chr 7	NC_000007.13:g.148958716_148958731=	NC_000007.13:g.148958726_148958731del	NC_000007.13:g.148958727_148958731del	NC_000007.13:g.148958729_148958731del	NC_000007.13:g.148958730_148958731del	NC_000007.13:g.148958731del	NC_000007.13:g.148958731dup	NC_000007.13:g.148958730_148958731dup	NC_000007.13:g.148958729_148958731dup

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#.

49 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43056707	Mar 14, 2006 (126)
2	HGSV	ss81853335	Dec 14, 2007 (130)
3	BCMHGSC_JDW	ss103760712	Dec 01, 2009 (131)
4	BUSHMAN	ss193953300	Apr 25, 2013 (138)
5	GMI	ss288880391	May 04, 2012 (137)
6	SSMP	ss663756409	Apr 01, 2015 (144)
7	EVA_GENOME_DK	ss1577113976	Apr 01, 2015 (144)
8	SWEGEN	ss3002272985	Nov 08, 2017 (151)
9	MCHAISSO	ss3064280520	Nov 08, 2017 (151)
10	MCHAISSO	ss3066177675	Nov 08, 2017 (151)
11	BEROUKHIMLAB	ss3644251612	Oct 12, 2018 (152)
12	EVA_DECODE	ss3720968350	Jul 13, 2019 (153)
13	EVA_DECODE	ss3720968351	Jul 13, 2019 (153)
14	EVA_DECODE	ss3720968352	Jul 13, 2019 (153)
15	EVA_DECODE	ss3720968353	Jul 13, 2019 (153)
16	ACPOP	ss3735191773	Jul 13, 2019 (153)
17	PACBIO	ss3785998010	Jul 13, 2019 (153)
18	EVA	ss3830891087	Apr 26, 2020 (154)
19	EVA	ss3838945044	Apr 26, 2020 (154)
20	EVA	ss3844402510	Apr 26, 2020 (154)
21	KOGIC	ss3962844606	Apr 26, 2020 (154)
22	KOGIC	ss3962844607	Apr 26, 2020 (154)
23	KOGIC	ss3962844608	Apr 26, 2020 (154)
24	KOGIC	ss3962844609	Apr 26, 2020 (154)
25	GNOMAD	ss4175570807	Apr 26, 2021 (155)
26	GNOMAD	ss4175570808	Apr 26, 2021 (155)
27	GNOMAD	ss4175570809	Apr 26, 2021 (155)
28	GNOMAD	ss4175570810	Apr 26, 2021 (155)
29	GNOMAD	ss4175570811	Apr 26, 2021 (155)
30	GNOMAD	ss4175570812	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5186222555	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5186222556	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5186222557	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5186222558	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5275240493	Oct 15, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5275240494	Oct 15, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5275240495	Oct 15, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5275240496	Oct 15, 2022 (156)
39	HUGCELL_USP	ss5472065185	Oct 15, 2022 (156)
40	HUGCELL_USP	ss5472065186	Oct 15, 2022 (156)
41	HUGCELL_USP	ss5472065187	Oct 15, 2022 (156)
42	HUGCELL_USP	ss5472065188	Oct 15, 2022 (156)
43	TOMMO_GENOMICS	ss5727421487	Oct 15, 2022 (156)
44	TOMMO_GENOMICS	ss5727421488	Oct 15, 2022 (156)
45	TOMMO_GENOMICS	ss5727421489	Oct 15, 2022 (156)
46	TOMMO_GENOMICS	ss5727421490	Oct 15, 2022 (156)
47	TOMMO_GENOMICS	ss5727421491	Oct 15, 2022 (156)
48	EVA	ss5823715605	Oct 15, 2022 (156)
49	EVA	ss5823715606	Oct 15, 2022 (156)
50	The Danish reference pan genome	NC_000007.13 - 148958716	Apr 26, 2020 (154)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280729825 (NC_000007.14:149261624::A 148/128126) Row 280729826 (NC_000007.14:149261624::AA 1/128172) Row 280729827 (NC_000007.14:149261624::AAA 1/128172)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 19222607 (NC_000007.14:149261625:AA: 897/1828) Row 19222608 (NC_000007.14:149261626:A: 93/1828) Row 19222609 (NC_000007.14:149261624:AAA: 35/1828)...	-	Apr 26, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 19222607 (NC_000007.14:149261625:AA: 897/1828) Row 19222608 (NC_000007.14:149261626:A: 93/1828) Row 19222609 (NC_000007.14:149261624:AAA: 35/1828)...	-	Apr 26, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 19222607 (NC_000007.14:149261625:AA: 897/1828) Row 19222608 (NC_000007.14:149261626:A: 93/1828) Row 19222609 (NC_000007.14:149261624:AAA: 35/1828)...	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 19222607 (NC_000007.14:149261625:AA: 897/1828) Row 19222608 (NC_000007.14:149261626:A: 93/1828) Row 19222609 (NC_000007.14:149261624:AAA: 35/1828)...	-	Apr 26, 2020 (154)
62	Northern Sweden	NC_000007.13 - 148958716	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 44191862 (NC_000007.13:148958715:AA: 9092/16758) Row 44191863 (NC_000007.13:148958715:A: 16/16758) Row 44191864 (NC_000007.13:148958715:AAA: 47/16758)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 44191862 (NC_000007.13:148958715:AA: 9092/16758) Row 44191863 (NC_000007.13:148958715:A: 16/16758) Row 44191864 (NC_000007.13:148958715:AAA: 47/16758)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 44191862 (NC_000007.13:148958715:AA: 9092/16758) Row 44191863 (NC_000007.13:148958715:A: 16/16758) Row 44191864 (NC_000007.13:148958715:AAA: 47/16758)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 44191862 (NC_000007.13:148958715:AA: 9092/16758) Row 44191863 (NC_000007.13:148958715:A: 16/16758) Row 44191864 (NC_000007.13:148958715:AAA: 47/16758)...	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 61258591 (NC_000007.14:149261624:AA: 15349/28258) Row 61258592 (NC_000007.14:149261624:AAA: 92/28258) Row 61258593 (NC_000007.14:149261624:A: 29/28258)...	-	Oct 15, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 61258591 (NC_000007.14:149261624:AA: 15349/28258) Row 61258592 (NC_000007.14:149261624:AAA: 92/28258) Row 61258593 (NC_000007.14:149261624:A: 29/28258)...	-	Oct 15, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 61258591 (NC_000007.14:149261624:AA: 15349/28258) Row 61258592 (NC_000007.14:149261624:AAA: 92/28258) Row 61258593 (NC_000007.14:149261624:A: 29/28258)...	-	Oct 15, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 61258591 (NC_000007.14:149261624:AA: 15349/28258) Row 61258592 (NC_000007.14:149261624:AAA: 92/28258) Row 61258593 (NC_000007.14:149261624:A: 29/28258)...	-	Oct 15, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 61258591 (NC_000007.14:149261624:AA: 15349/28258) Row 61258592 (NC_000007.14:149261624:AAA: 92/28258) Row 61258593 (NC_000007.14:149261624:A: 29/28258)...	-	Oct 15, 2022 (156)
72	ALFA	NC_000007.14 - 149261625	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)
rs58113375	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4175570812	NC_000007.14:149261624:AAAAAA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3002272985, ss5186222557, ss5823715606	NC_000007.13:148958715:AAA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3720968353, ss3962844608, ss4175570811, ss5275240496, ss5472065187, ss5727421488	NC_000007.14:149261624:AAA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss81853335	NC_000007.11:148396377:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss288880391	NC_000007.12:148589648:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1192702, 8476638, ss663756409, ss1577113976, ss3644251612, ss3735191773, ss3830891087, ss3838945044, ss5186222555, ss5823715605	NC_000007.13:148958715:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3064280520, ss3066177675, ss3844402510, ss4175570810, ss5275240494, ss5472065185, ss5727421487	NC_000007.14:149261624:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3720968352, ss3962844606	NC_000007.14:149261625:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss43056707, ss103760712	NT_007914.15:9554352:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193953300	NT_007933.16:86754845:AA:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3785998010, ss5186222556	NC_000007.13:148958715:A:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5275240493, ss5472065186, ss5727421489	NC_000007.14:149261624:A:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3720968351, ss3962844607	NC_000007.14:149261626:A:	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5186222558	NC_000007.13:148958715::A	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4175570807, ss5275240495, ss5472065188, ss5727421490	NC_000007.14:149261624::A	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12708150461	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3720968350, ss3962844609	NC_000007.14:149261627::A	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4175570808, ss5727421491	NC_000007.14:149261624::AA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4175570809	NC_000007.14:149261624::AAA	NC_000007.14:149261624:AAAAAAAAAAA… NC_000007.14:149261624:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(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 rs34630774

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

rs34630774