Name: rs34056277
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.

rs34056277

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:136727245-136727263 (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)₉ / del(A)₇ / del(A)₆ / del(…
del(A)₉ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.0766 (682/8902, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SNHG7 : Intron Variant
SNORA17A : 2KB Upstream Variant
SNORA17B : 2KB Upstream Variant (+ 1 more)
LOC124900276 : 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	8902	AAAAAAAAAAAAAAAAAAA=0.8943	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0271, AAAAAAAAAAAAAAAA=0.0015, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0766, AAAAAAAAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.868459	0.019505	0.112036	32
European	Sub	7508	AAAAAAAAAAAAAAAAAAA=0.8749	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0321, AAAAAAAAAAAAAAAA=0.0017, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0906, AAAAAAAAAAAAAAAAAAAA=0.0007, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.842886	0.023382	0.133733	32
African	Sub	916	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	40	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	876	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	54	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	174	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	164	AAAAAAAAAAAAAAAAAAA=0.988	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.012, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	0.97561	0.0	0.02439	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	8902	(A)₁₉=0.8943	del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0271, delAAA=0.0015, delAA=0.0000, delA=0.0766, dupA=0.0006, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	7508	(A)₁₉=0.8749	del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0321, delAAA=0.0017, delAA=0.0000, delA=0.0906, dupA=0.0007, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	916	(A)₁₉=1.000	del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	174	(A)₁₉=1.000	del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	164	(A)₁₉=0.988	del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.012, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	56	(A)₁₉=1.00	del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	54	(A)₁₉=1.00	del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(A)₁₉=1.00	del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=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 9	NC_000009.12:g.136727255_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727257_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727258_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727259_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727260_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727261_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727262_136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727263del
GRCh38.p14 chr 9	NC_000009.12:g.136727263dup
GRCh38.p14 chr 9	NC_000009.12:g.136727262_136727263dup
GRCh38.p14 chr 9	NC_000009.12:g.136727261_136727263dup
GRCh38.p14 chr 9	NC_000009.12:g.136727260_136727263dup
GRCh37.p13 chr 9	NC_000009.11:g.139621707_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621709_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621710_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621711_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621712_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621713_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621714_139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621715del
GRCh37.p13 chr 9	NC_000009.11:g.139621715dup
GRCh37.p13 chr 9	NC_000009.11:g.139621714_139621715dup
GRCh37.p13 chr 9	NC_000009.11:g.139621713_139621715dup
GRCh37.p13 chr 9	NC_000009.11:g.139621712_139621715dup

Gene: SNHG7, small nucleolar RNA host gene 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SNHG7 transcript variant 1	NR_003672.2:n.	N/A	Intron Variant
SNHG7 transcript variant 2	NR_024542.1:n.	N/A	Intron Variant
SNHG7 transcript variant 3	NR_024543.1:n.	N/A	Intron Variant

Gene: SNORA17A, small nucleolar RNA, H/ACA box 17A (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SNORA17A transcript	NR_002958.1:n.	N/A	Upstream Transcript Variant

Gene: SNORA17B, small nucleolar RNA, H/ACA box 17B (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SNORA17B transcript	NR_002975.2:n.	N/A	Upstream Transcript Variant

Gene: LOC124900276, uncharacterized LOC124900276 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124900276 transcript	XM_047424334.1:c.-3928-16… XM_047424334.1:c.-3928-167_-3928-159del	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)₁₉=	del(A)₉	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 9	NC_000009.12:g.136727245_136727263=	NC_000009.12:g.136727255_136727263del	NC_000009.12:g.136727257_136727263del	NC_000009.12:g.136727258_136727263del	NC_000009.12:g.136727259_136727263del	NC_000009.12:g.136727260_136727263del	NC_000009.12:g.136727261_136727263del	NC_000009.12:g.136727262_136727263del	NC_000009.12:g.136727263del	NC_000009.12:g.136727263dup	NC_000009.12:g.136727262_136727263dup	NC_000009.12:g.136727261_136727263dup	NC_000009.12:g.136727260_136727263dup
GRCh37.p13 chr 9	NC_000009.11:g.139621697_139621715=	NC_000009.11:g.139621707_139621715del	NC_000009.11:g.139621709_139621715del	NC_000009.11:g.139621710_139621715del	NC_000009.11:g.139621711_139621715del	NC_000009.11:g.139621712_139621715del	NC_000009.11:g.139621713_139621715del	NC_000009.11:g.139621714_139621715del	NC_000009.11:g.139621715del	NC_000009.11:g.139621715dup	NC_000009.11:g.139621714_139621715dup	NC_000009.11:g.139621713_139621715dup	NC_000009.11:g.139621712_139621715dup
LOC124900276 transcript	XM_047424334.1:c.-3928-159=	XM_047424334.1:c.-3928-167_-3928-159del	XM_047424334.1:c.-3928-165_-3928-159del	XM_047424334.1:c.-3928-164_-3928-159del	XM_047424334.1:c.-3928-163_-3928-159del	XM_047424334.1:c.-3928-162_-3928-159del	XM_047424334.1:c.-3928-161_-3928-159del	XM_047424334.1:c.-3928-160_-3928-159del	XM_047424334.1:c.-3928-159del	XM_047424334.1:c.-3928-159dup	XM_047424334.1:c.-3928-160_-3928-159dup	XM_047424334.1:c.-3928-161_-3928-159dup	XM_047424334.1:c.-3928-162_-3928-159dup

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#.

41 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43378045	Mar 13, 2006 (126)
2	HGSV	ss80350841	Dec 14, 2007 (129)
3	BCMHGSC_JDW	ss103790394	Mar 15, 2016 (147)
4	BILGI_BIOE	ss666486215	Jan 10, 2018 (151)
5	1000GENOMES	ss1368953049	Aug 21, 2014 (144)
6	SYSTEMSBIOZJU	ss2627429921	Nov 08, 2017 (151)
7	SWEGEN	ss3005759392	Nov 08, 2017 (151)
8	BEROUKHIMLAB	ss3644290543	Oct 12, 2018 (152)
9	BEROUKHIMLAB	ss3644290544	Oct 12, 2018 (152)
10	EVA_DECODE	ss3724963954	Jul 13, 2019 (153)
11	EVA_DECODE	ss3724963955	Jul 13, 2019 (153)
12	EVA_DECODE	ss3724963956	Jul 13, 2019 (153)
13	EVA_DECODE	ss3724963957	Jul 13, 2019 (153)
14	ACPOP	ss3736964374	Jul 13, 2019 (153)
15	ACPOP	ss3736964375	Jul 13, 2019 (153)
16	EVA	ss3831911656	Apr 26, 2020 (154)
17	EVA	ss3844950475	Apr 26, 2020 (154)
18	GNOMAD	ss4211185812	Apr 26, 2021 (155)
19	GNOMAD	ss4211185813	Apr 26, 2021 (155)
20	GNOMAD	ss4211185814	Apr 26, 2021 (155)
21	GNOMAD	ss4211185815	Apr 26, 2021 (155)
22	GNOMAD	ss4211185818	Apr 26, 2021 (155)
23	GNOMAD	ss4211185819	Apr 26, 2021 (155)
24	GNOMAD	ss4211185820	Apr 26, 2021 (155)
25	GNOMAD	ss4211185821	Apr 26, 2021 (155)
26	GNOMAD	ss4211185822	Apr 26, 2021 (155)
27	GNOMAD	ss4211185823	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5195777642	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5195777643	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5195777644	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5282547143	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5282547144	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5282547145	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5478372049	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5478372050	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5478372051	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5478372052	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5740475854	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5740475855	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5740475856	Oct 16, 2022 (156)
41	EVA	ss5856977908	Oct 16, 2022 (156)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 340548585 (NC_000009.12:136727244::A 994/119392) Row 340548586 (NC_000009.12:136727244::AA 45/119412) Row 340548587 (NC_000009.12:136727244::AAA 1105/119382)...	-	Apr 26, 2021 (155)
53	Northern Sweden Submission ignored due to conflicting rows: Row 10249239 (NC_000009.11:139621696:A: 77/582) Row 10249240 (NC_000009.11:139621696:AAAA: 56/582)	-	Jul 13, 2019 (153)
54	Northern Sweden Submission ignored due to conflicting rows: Row 10249239 (NC_000009.11:139621696:A: 77/582) Row 10249240 (NC_000009.11:139621696:AAAA: 56/582)	-	Jul 13, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 53746949 (NC_000009.11:139621696:A: 2339/16730) Row 53746950 (NC_000009.11:139621696:AA: 11/16730) Row 53746951 (NC_000009.11:139621696::A 101/16730)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 53746949 (NC_000009.11:139621696:A: 2339/16730) Row 53746950 (NC_000009.11:139621696:AA: 11/16730) Row 53746951 (NC_000009.11:139621696::A 101/16730)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 53746949 (NC_000009.11:139621696:A: 2339/16730) Row 53746950 (NC_000009.11:139621696:AA: 11/16730) Row 53746951 (NC_000009.11:139621696::A 101/16730)	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 74312958 (NC_000009.12:136727244:A: 4302/28244) Row 74312959 (NC_000009.12:136727244::A 162/28244) Row 74312960 (NC_000009.12:136727244:AA: 15/28244)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 74312958 (NC_000009.12:136727244:A: 4302/28244) Row 74312959 (NC_000009.12:136727244::A 162/28244) Row 74312960 (NC_000009.12:136727244:AA: 15/28244)	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 74312958 (NC_000009.12:136727244:A: 4302/28244) Row 74312959 (NC_000009.12:136727244::A 162/28244) Row 74312960 (NC_000009.12:136727244:AA: 15/28244)	-	Oct 16, 2022 (156)
61	ALFA	NC_000009.12 - 136727245	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)
rs78377592	May 11, 2012 (137)
rs528314054	Apr 01, 2015 (144)
rs796923352	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4211185823	NC_000009.12:136727244:AAAAAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4211185822	NC_000009.12:136727244:AAAAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3724963957, ss4211185821	NC_000009.12:136727244:AAAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3005759392, ss3736964375	NC_000009.11:139621696:AAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4211185820, ss5282547145, ss5478372052	NC_000009.12:136727244:AAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3724963956	NC_000009.12:136727245:AAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss103790394	NT_024000.16:404714:AAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4211185819	NC_000009.12:136727244:AAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss666486215, ss3644290544, ss5195777643	NC_000009.11:139621696:AA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3844950475, ss4211185818, ss5282547144, ss5478372051, ss5740475856	NC_000009.12:136727244:AA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3724963955	NC_000009.12:136727247:AA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss2627429921, ss3644290543, ss3736964374, ss3831911656, ss5195777642	NC_000009.11:139621696:A:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5282547143, ss5478372050, ss5740475854, ss5856977908	NC_000009.12:136727244:A:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3724963954	NC_000009.12:136727248:A:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss43378045	NT_024000.16:404699:A:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5195777644	NC_000009.11:139621696::A	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4211185812, ss5478372049, ss5740475855	NC_000009.12:136727244::A	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss80350841	NT_024000.16:404718::A	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4211185813	NC_000009.12:136727244::AA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4211185814	NC_000009.12:136727244::AAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1368953049	NC_000009.11:139621697::AAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4211185815	NC_000009.12:136727244::AAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
271897093	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3603197667	NC_000009.12:136727244:AAAAAAAAA:	NC_000009.12:136727244:AAAAAAAAAAA… NC_000009.12:136727244:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

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

No publications for rs34056277

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

rs34056277