Name: rs34604391
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.

rs34604391

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:5188751-5188765 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.4416 (2489/5636, ALFA)
dupT=0.4579 (2293/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF594 : 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	5636	TTTTTTTTTTTTTTT=0.5584	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.4416, TTTTTTTTTTTTTTTTT=0.0000	0.429383	0.312633	0.257984	32
European	Sub	4936	TTTTTTTTTTTTTTT=0.4968	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.5032, TTTTTTTTTTTTTTTTT=0.0000	0.349676	0.356159	0.294165	32
African	Sub	464	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	442	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	54	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	10	TTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	64	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	58	TTTTTTTTTTTTTTT=0.91	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTT=0.00	0.896552	0.068966	0.034483	10

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
Allele Frequency Aggregator	Total	Global	5636	(T)₁₅=0.5584	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.4416, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	4936	(T)₁₅=0.4968	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.5032, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	464	(T)₁₅=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	64	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Other	Sub	58	(T)₁₅=0.91	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.09, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	54	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(T)₁₅=1.0	del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.4579
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.4652
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3095
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.6183
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.312
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.633

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 17	NC_000017.11:g.5188762_5188765del
GRCh38.p14 chr 17	NC_000017.11:g.5188763_5188765del
GRCh38.p14 chr 17	NC_000017.11:g.5188764_5188765del
GRCh38.p14 chr 17	NC_000017.11:g.5188765del
GRCh38.p14 chr 17	NC_000017.11:g.5188765dup
GRCh38.p14 chr 17	NC_000017.11:g.5188764_5188765dup
GRCh38.p14 chr 17	NC_000017.11:g.5188763_5188765dup
GRCh38.p14 chr 17	NC_000017.11:g.5188756_5188765dup
GRCh37.p13 chr 17	NC_000017.10:g.5092057_5092060del
GRCh37.p13 chr 17	NC_000017.10:g.5092058_5092060del
GRCh37.p13 chr 17	NC_000017.10:g.5092059_5092060del
GRCh37.p13 chr 17	NC_000017.10:g.5092060del
GRCh37.p13 chr 17	NC_000017.10:g.5092060dup
GRCh37.p13 chr 17	NC_000017.10:g.5092059_5092060dup
GRCh37.p13 chr 17	NC_000017.10:g.5092058_5092060dup
GRCh37.p13 chr 17	NC_000017.10:g.5092051_5092060dup

Gene: ZNF594, zinc finger protein 594 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF594 transcript	NM_032530.2:c.-21+2994_-2… NM_032530.2:c.-21+2994_-21+2997del	N/A	Intron Variant
ZNF594 transcript variant X1	XM_005256827.4:c.-21+2678… XM_005256827.4:c.-21+2678_-21+2681del	N/A	Intron Variant
ZNF594 transcript variant X2	XR_001752666.3:n.	N/A	Intron Variant
ZNF594 transcript variant X5	XR_001752667.3:n.	N/A	Intron Variant
ZNF594 transcript variant X3	XR_007065504.1:n.	N/A	Intron Variant
ZNF594 transcript variant X4	XR_007065505.1: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)₁₅=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₁₀
GRCh38.p14 chr 17	NC_000017.11:g.5188751_5188765=	NC_000017.11:g.5188762_5188765del	NC_000017.11:g.5188763_5188765del	NC_000017.11:g.5188764_5188765del	NC_000017.11:g.5188765del	NC_000017.11:g.5188765dup	NC_000017.11:g.5188764_5188765dup	NC_000017.11:g.5188763_5188765dup	NC_000017.11:g.5188756_5188765dup
GRCh37.p13 chr 17	NC_000017.10:g.5092046_5092060=	NC_000017.10:g.5092057_5092060del	NC_000017.10:g.5092058_5092060del	NC_000017.10:g.5092059_5092060del	NC_000017.10:g.5092060del	NC_000017.10:g.5092060dup	NC_000017.10:g.5092059_5092060dup	NC_000017.10:g.5092058_5092060dup	NC_000017.10:g.5092051_5092060dup
ZNF594 transcript	NM_032530.1:c.-21+2997=	NM_032530.1:c.-21+2994_-21+2997del	NM_032530.1:c.-21+2995_-21+2997del	NM_032530.1:c.-21+2996_-21+2997del	NM_032530.1:c.-21+2997del	NM_032530.1:c.-21+2997dup	NM_032530.1:c.-21+2996_-21+2997dup	NM_032530.1:c.-21+2995_-21+2997dup	NM_032530.1:c.-21+2988_-21+2997dup
ZNF594 transcript	NM_032530.2:c.-21+2997=	NM_032530.2:c.-21+2994_-21+2997del	NM_032530.2:c.-21+2995_-21+2997del	NM_032530.2:c.-21+2996_-21+2997del	NM_032530.2:c.-21+2997del	NM_032530.2:c.-21+2997dup	NM_032530.2:c.-21+2996_-21+2997dup	NM_032530.2:c.-21+2995_-21+2997dup	NM_032530.2:c.-21+2988_-21+2997dup
ZNF594 transcript variant X1	XM_005256827.1:c.-21+2681=	XM_005256827.1:c.-21+2678_-21+2681del	XM_005256827.1:c.-21+2679_-21+2681del	XM_005256827.1:c.-21+2680_-21+2681del	XM_005256827.1:c.-21+2681del	XM_005256827.1:c.-21+2681dup	XM_005256827.1:c.-21+2680_-21+2681dup	XM_005256827.1:c.-21+2679_-21+2681dup	XM_005256827.1:c.-21+2672_-21+2681dup
ZNF594 transcript variant X1	XM_005256827.4:c.-21+2681=	XM_005256827.4:c.-21+2678_-21+2681del	XM_005256827.4:c.-21+2679_-21+2681del	XM_005256827.4:c.-21+2680_-21+2681del	XM_005256827.4:c.-21+2681del	XM_005256827.4:c.-21+2681dup	XM_005256827.4:c.-21+2680_-21+2681dup	XM_005256827.4:c.-21+2679_-21+2681dup	XM_005256827.4:c.-21+2672_-21+2681dup

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, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40834878	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95687150	Dec 05, 2013 (138)
3	PJP	ss294902583	May 09, 2011 (135)
4	SSMP	ss664363156	Apr 01, 2015 (144)
5	BILGI_BIOE	ss666682607	Apr 25, 2013 (138)
6	SSIP	ss947363792	Oct 12, 2018 (152)
7	1000GENOMES	ss1376325152	Aug 21, 2014 (142)
8	SWEGEN	ss3015124537	Nov 08, 2017 (151)
9	SWEGEN	ss3015124538	Nov 08, 2017 (151)
10	URBANLAB	ss3650593702	Oct 12, 2018 (152)
11	EVA_DECODE	ss3699998930	Jul 13, 2019 (153)
12	EVA_DECODE	ss3699998931	Jul 13, 2019 (153)
13	EVA_DECODE	ss3699998932	Jul 13, 2019 (153)
14	EVA_DECODE	ss3699998933	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699998934	Jul 13, 2019 (153)
16	PACBIO	ss3788137319	Jul 13, 2019 (153)
17	PACBIO	ss3793107323	Jul 13, 2019 (153)
18	PACBIO	ss3797992920	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3819667248	Jul 13, 2019 (153)
20	EVA	ss3834756145	Apr 27, 2020 (154)
21	EVA	ss3840986256	Apr 27, 2020 (154)
22	EVA	ss3846480519	Apr 27, 2020 (154)
23	KOGIC	ss3978311094	Apr 27, 2020 (154)
24	KOGIC	ss3978311095	Apr 27, 2020 (154)
25	KOGIC	ss3978311096	Apr 27, 2020 (154)
26	GNOMAD	ss4307242624	Apr 27, 2021 (155)
27	GNOMAD	ss4307242625	Apr 27, 2021 (155)
28	GNOMAD	ss4307242626	Apr 27, 2021 (155)
29	GNOMAD	ss4307242628	Apr 27, 2021 (155)
30	GNOMAD	ss4307242629	Apr 27, 2021 (155)
31	GNOMAD	ss4307242630	Apr 27, 2021 (155)
32	GNOMAD	ss4307242631	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5221298163	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5221298164	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5221298165	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5221298166	Apr 27, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5302275504	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5302275505	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5302275506	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5495465875	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5495465876	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5495465877	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5776833989	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5776833990	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5776833991	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5776833993	Oct 16, 2022 (156)
47	EVA	ss5833661605	Oct 16, 2022 (156)
48	EVA	ss5833661606	Oct 16, 2022 (156)
49	EVA	ss5851720051	Oct 16, 2022 (156)
50	EVA	ss5913058131	Oct 16, 2022 (156)
51	1000Genomes	NC_000017.10 - 5092046	Oct 12, 2018 (152)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500277517 (NC_000017.11:5188750::T 86188/129358) Row 500277518 (NC_000017.11:5188750::TT 224/129334) Row 500277519 (NC_000017.11:5188750::TTT 6/129370)...	-	Apr 27, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 34689095 (NC_000017.11:5188750:T: 35/1832) Row 34689096 (NC_000017.11:5188751::T 453/1832) Row 34689097 (NC_000017.11:5188751::TT 14/1832)	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 34689095 (NC_000017.11:5188750:T: 35/1832) Row 34689096 (NC_000017.11:5188751::T 453/1832) Row 34689097 (NC_000017.11:5188751::TT 14/1832)	-	Apr 27, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 34689095 (NC_000017.11:5188750:T: 35/1832) Row 34689096 (NC_000017.11:5188751::T 453/1832) Row 34689097 (NC_000017.11:5188751::TT 14/1832)	-	Apr 27, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 79267470 (NC_000017.10:5092045::T 3405/16752) Row 79267471 (NC_000017.10:5092045:T: 21/16752) Row 79267472 (NC_000017.10:5092045::TT 2/16752)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 79267470 (NC_000017.10:5092045::T 3405/16752) Row 79267471 (NC_000017.10:5092045:T: 21/16752) Row 79267472 (NC_000017.10:5092045::TT 2/16752)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 79267470 (NC_000017.10:5092045::T 3405/16752) Row 79267471 (NC_000017.10:5092045:T: 21/16752) Row 79267472 (NC_000017.10:5092045::TT 2/16752)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 79267470 (NC_000017.10:5092045::T 3405/16752) Row 79267471 (NC_000017.10:5092045:T: 21/16752) Row 79267472 (NC_000017.10:5092045::TT 2/16752)...	-	Apr 27, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 110671093 (NC_000017.11:5188750::T 5856/28258) Row 110671094 (NC_000017.11:5188750::TT 1/28258) Row 110671095 (NC_000017.11:5188750:T: 19/28258)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 110671093 (NC_000017.11:5188750::T 5856/28258) Row 110671094 (NC_000017.11:5188750::TT 1/28258) Row 110671095 (NC_000017.11:5188750:T: 19/28258)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 110671093 (NC_000017.11:5188750::T 5856/28258) Row 110671094 (NC_000017.11:5188750::TT 1/28258) Row 110671095 (NC_000017.11:5188750:T: 19/28258)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 110671093 (NC_000017.11:5188750::T 5856/28258) Row 110671094 (NC_000017.11:5188750::TT 1/28258) Row 110671095 (NC_000017.11:5188750:T: 19/28258)...	-	Oct 16, 2022 (156)
70	ALFA	NC_000017.11 - 5188751	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)
rs66868158	May 11, 2012 (137)
rs66868159	Feb 26, 2009 (130)
rs146585318	Sep 17, 2011 (135)
rs376147097	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4307242631	NC_000017.11:5188750:TTTT:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5221298166	NC_000017.10:5092045:TTT:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4307242630, ss5776833993	NC_000017.11:5188750:TTT:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3699998930, ss4307242629	NC_000017.11:5188750:TT:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5221298164	NC_000017.10:5092045:T:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3978311094, ss4307242628, ss5302275505, ss5495465877, ss5776833991	NC_000017.11:5188750:T:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3699998931	NC_000017.11:5188751:T:	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss294902583	NC_000017.9:5032784::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
70945177, ss664363156, ss666682607, ss1376325152, ss3015124537, ss3788137319, ss3793107323, ss3797992920, ss3834756145, ss3840986256, ss5221298163, ss5833661605	NC_000017.10:5092045::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss947363792	NC_000017.10:5092046::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3650593702, ss3819667248, ss3846480519, ss4307242624, ss5302275504, ss5495465875, ss5776833989, ss5851720051, ss5913058131	NC_000017.11:5188750::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3978311095	NC_000017.11:5188751::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3699998932	NC_000017.11:5188752::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss40834878, ss95687150	NT_010718.16:4695434::T	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3015124538, ss5221298165, ss5833661606	NC_000017.10:5092045::TT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4307242625, ss5302275506, ss5495465876, ss5776833990	NC_000017.11:5188750::TT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9382380459	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3978311096	NC_000017.11:5188751::TT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3699998933	NC_000017.11:5188752::TT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4307242626	NC_000017.11:5188750::TTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3699998934	NC_000017.11:5188752::TTTTTTTTTT	NC_000017.11:5188750:TTTTTTTTTTTTT… NC_000017.11:5188750:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34604391

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

rs34604391