Name: rs1234826386
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.

rs1234826386

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:775841-775860 (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 / del(A)₄ / delA…
del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₇ / dup(A)₁₁ / dup(A)₁₇ / insAAC(A)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₅=0.000 (0/920, ALFA)
del(A)₄=0.000 (0/920, ALFA)
delAAA=0.000 (0/920, ALFA) (+ 7 more)
delAA=0.000 (0/920, ALFA)
delA=0.000 (0/920, ALFA)
dupA=0.000 (0/920, ALFA)
dupAA=0.000 (0/920, ALFA)
dupAAA=0.000 (0/920, ALFA)
dup(A)₄=0.000 (0/920, ALFA)
dup(A)₅=0.000 (0/920, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC100288069 : 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	920	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	252	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	536	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	504	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	10	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	20	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	52	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	46	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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	920	(A)₂₀=1.000	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, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	536	(A)₂₀=1.000	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, dup(A)₅=0.000
Allele Frequency Aggregator	European	Sub	252	(A)₂₀=1.000	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, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	52	(A)₂₀=1.00	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, dup(A)₅=0.00
Allele Frequency Aggregator	Other	Sub	46	(A)₂₀=1.00	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, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(A)₂₀=1.00	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, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	10	(A)₂₀=1.0	del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₀=1.0	del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=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 1	NC_000001.11:g.775855_775860del
GRCh38.p14 chr 1	NC_000001.11:g.775856_775860del
GRCh38.p14 chr 1	NC_000001.11:g.775857_775860del
GRCh38.p14 chr 1	NC_000001.11:g.775858_775860del
GRCh38.p14 chr 1	NC_000001.11:g.775859_775860del
GRCh38.p14 chr 1	NC_000001.11:g.775860del
GRCh38.p14 chr 1	NC_000001.11:g.775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775859_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775858_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775857_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775856_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775854_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775850_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775844_775860dup
GRCh38.p14 chr 1	NC_000001.11:g.775841_775860A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 1	NC_000001.10:g.711235_711240del
GRCh37.p13 chr 1	NC_000001.10:g.711236_711240del
GRCh37.p13 chr 1	NC_000001.10:g.711237_711240del
GRCh37.p13 chr 1	NC_000001.10:g.711238_711240del
GRCh37.p13 chr 1	NC_000001.10:g.711239_711240del
GRCh37.p13 chr 1	NC_000001.10:g.711240del
GRCh37.p13 chr 1	NC_000001.10:g.711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711239_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711238_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711237_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711236_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711234_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711230_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711224_711240dup
GRCh37.p13 chr 1	NC_000001.10:g.711221_711240A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Gene: LOC100288069, uncharacterized LOC100288069 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC100288069 transcript	NR_168328.1: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)₂₀=	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇	dup(A)₁₁	dup(A)₁₇	insAAC(A)₂₆
GRCh38.p14 chr 1	NC_000001.11:g.775841_775860=	NC_000001.11:g.775855_775860del	NC_000001.11:g.775856_775860del	NC_000001.11:g.775857_775860del	NC_000001.11:g.775858_775860del	NC_000001.11:g.775859_775860del	NC_000001.11:g.775860del	NC_000001.11:g.775860dup	NC_000001.11:g.775859_775860dup	NC_000001.11:g.775858_775860dup	NC_000001.11:g.775857_775860dup	NC_000001.11:g.775856_775860dup	NC_000001.11:g.775854_775860dup	NC_000001.11:g.775850_775860dup	NC_000001.11:g.775844_775860dup	NC_000001.11:g.775841_775860A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 1	NC_000001.10:g.711221_711240=	NC_000001.10:g.711235_711240del	NC_000001.10:g.711236_711240del	NC_000001.10:g.711237_711240del	NC_000001.10:g.711238_711240del	NC_000001.10:g.711239_711240del	NC_000001.10:g.711240del	NC_000001.10:g.711240dup	NC_000001.10:g.711239_711240dup	NC_000001.10:g.711238_711240dup	NC_000001.10:g.711237_711240dup	NC_000001.10:g.711236_711240dup	NC_000001.10:g.711234_711240dup	NC_000001.10:g.711230_711240dup	NC_000001.10:g.711224_711240dup	NC_000001.10:g.711221_711240A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

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#.

43 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2986147557	Jan 10, 2018 (151)
2	SWEGEN	ss2986147559	Jan 10, 2018 (151)
3	URBANLAB	ss3646581096	Oct 11, 2018 (152)
4	EVA_DECODE	ss3685991570	Jul 12, 2019 (153)
5	EVA_DECODE	ss3685991571	Jul 12, 2019 (153)
6	EVA_DECODE	ss3685991572	Jul 12, 2019 (153)
7	EVA_DECODE	ss3685991573	Jul 12, 2019 (153)
8	EVA_DECODE	ss3685991574	Jul 12, 2019 (153)
9	EVA_DECODE	ss3685991575	Jul 12, 2019 (153)
10	PACBIO	ss3788979904	Jul 12, 2019 (153)
11	PACBIO	ss3788979905	Jul 12, 2019 (153)
12	PACBIO	ss3793852441	Jul 12, 2019 (153)
13	PACBIO	ss3793852442	Jul 12, 2019 (153)
14	EVA	ss3825981365	Apr 25, 2020 (154)
15	GNOMAD	ss3986920393	Apr 25, 2021 (155)
16	GNOMAD	ss3986920394	Apr 25, 2021 (155)
17	GNOMAD	ss3986920395	Apr 25, 2021 (155)
18	GNOMAD	ss3986920396	Apr 25, 2021 (155)
19	GNOMAD	ss3986920397	Apr 25, 2021 (155)
20	GNOMAD	ss3986920398	Apr 25, 2021 (155)
21	GNOMAD	ss3986920399	Apr 25, 2021 (155)
22	GNOMAD	ss3986920400	Apr 25, 2021 (155)
23	GNOMAD	ss3986920401	Apr 25, 2021 (155)
24	GNOMAD	ss3986920406	Apr 25, 2021 (155)
25	GNOMAD	ss3986920407	Apr 25, 2021 (155)
26	GNOMAD	ss3986920408	Apr 25, 2021 (155)
27	GNOMAD	ss3986920409	Apr 25, 2021 (155)
28	GNOMAD	ss3986920410	Apr 25, 2021 (155)
29	TOMMO_GENOMICS	ss5142049158	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5142049159	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5142049160	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5142049161	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5142049162	Apr 25, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5240861206	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5240861207	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5240861208	Oct 12, 2022 (156)
37	SANFORD_IMAGENETICS	ss5624747745	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5666187333	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5666187334	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5666187335	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5666187336	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5666187337	Oct 12, 2022 (156)
43	EVA	ss5831417571	Oct 12, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 52457 (NC_000001.11:775840::A 51723/77310) Row 52458 (NC_000001.11:775840::AA 10507/76960) Row 52459 (NC_000001.11:775840::AAA 354/77166)...	-	Apr 25, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 18465 (NC_000001.10:711220::A 5996/14800) Row 18466 (NC_000001.10:711220:AAAA: 677/14800) Row 18467 (NC_000001.10:711220:A: 360/14800)...	-	Apr 25, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 18465 (NC_000001.10:711220::A 5996/14800) Row 18466 (NC_000001.10:711220:AAAA: 677/14800) Row 18467 (NC_000001.10:711220:A: 360/14800)...	-	Apr 25, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 18465 (NC_000001.10:711220::A 5996/14800) Row 18466 (NC_000001.10:711220:AAAA: 677/14800) Row 18467 (NC_000001.10:711220:A: 360/14800)...	-	Apr 25, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 18465 (NC_000001.10:711220::A 5996/14800) Row 18466 (NC_000001.10:711220:AAAA: 677/14800) Row 18467 (NC_000001.10:711220:A: 360/14800)...	-	Apr 25, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 18465 (NC_000001.10:711220::A 5996/14800) Row 18466 (NC_000001.10:711220:AAAA: 677/14800) Row 18467 (NC_000001.10:711220:A: 360/14800)...	-	Apr 25, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 24437 (NC_000001.11:775840::A 10314/26226) Row 24438 (NC_000001.11:775840:AAAA: 984/26226) Row 24439 (NC_000001.11:775840:A: 549/26226)...	-	Oct 12, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 24437 (NC_000001.11:775840::A 10314/26226) Row 24438 (NC_000001.11:775840:AAAA: 984/26226) Row 24439 (NC_000001.11:775840:A: 549/26226)...	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 24437 (NC_000001.11:775840::A 10314/26226) Row 24438 (NC_000001.11:775840:AAAA: 984/26226) Row 24439 (NC_000001.11:775840:A: 549/26226)...	-	Oct 12, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 24437 (NC_000001.11:775840::A 10314/26226) Row 24438 (NC_000001.11:775840:AAAA: 984/26226) Row 24439 (NC_000001.11:775840:A: 549/26226)...	-	Oct 12, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 24437 (NC_000001.11:775840::A 10314/26226) Row 24438 (NC_000001.11:775840:AAAA: 984/26226) Row 24439 (NC_000001.11:775840:A: 549/26226)...	-	Oct 12, 2022 (156)
69	ALFA	NC_000001.11 - 775841	Apr 25, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3986920410	NC_000001.11:775840:AAAAAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3986920409	NC_000001.11:775840:AAAAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5142049159	NC_000001.10:711220:AAAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3685991575, ss3986920408, ss5666187334	NC_000001.11:775840:AAAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3986920407, ss5666187337	NC_000001.11:775840:AAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3685991574	NC_000001.11:775841:AAA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3986920406	NC_000001.11:775840:AA:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5142049160	NC_000001.10:711220:A:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5240861206, ss5666187335	NC_000001.11:775840:A:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3685991573	NC_000001.11:775843:A:	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss2986147557, ss3788979904, ss3793852441, ss3825981365, ss5142049158, ss5624747745	NC_000001.10:711220::A	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3646581096, ss3986920393, ss5666187333	NC_000001.11:775840::A	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3685991572	NC_000001.11:775844::A	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss2986147559, ss3788979905, ss3793852442, ss5142049161, ss5831417571	NC_000001.10:711220::AA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920394, ss5666187336	NC_000001.11:775840::AA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3685991571	NC_000001.11:775844::AA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5142049162	NC_000001.10:711220::AAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920395, ss5240861207	NC_000001.11:775840::AAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920396, ss5240861208	NC_000001.11:775840::AAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920397	NC_000001.11:775840::AAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
551381997	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3685991570	NC_000001.11:775844::AAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920398	NC_000001.11:775840::AAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920399	NC_000001.11:775840::AAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920400	NC_000001.11:775840::AAAAAAAAAAAAA… NC_000001.11:775840::AAAAAAAAAAAAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3986920401	NC_000001.11:775840::AAAAAAAAAAAAA… NC_000001.11:775840::AAAAAAAAAAAAAAAAAAAAAACAAAAAA	NC_000001.11:775840:AAAAAAAAAAAAAA… NC_000001.11:775840:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1234826386

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

rs1234826386