Name: rs10569711
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.

rs10569711

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:66602264-66602280 (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(TA)₃ / delTATA / delTA / dupTA…
del(TA)₃ / delTATA / delTA / dupTA / dupTATA / dup(TA)₃ / dup(TA)₄ / dup(TA)₅ / dup(TA)₆
Variation Type: Indel Insertion and Deletion
Frequency: (AT)₈A=0.415358 (109941/264690, TOPMED)
(AT)₈A=0.3924 (2994/7629, ALFA)
(AT)₈A=0.19 (7/36, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01798 : 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	7629	ATATATATATATATATA=0.3924	ATATATATATATA=0.0000, ATATATATATATATA=0.5979, ATATATATATATATATATA=0.0096, ATATATATATATATATATATA=0.0001, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATA=0.0000	0.287237	0.451167	0.261596	32
European	Sub	6446	ATATATATATATATATA=0.2906	ATATATATATATA=0.0000, ATATATATATATATA=0.6980, ATATATATATATATATATA=0.0113, ATATATATATATATATATATA=0.0002, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATA=0.0000	0.157292	0.538889	0.303819	32
African	Sub	956	ATATATATATATATATA=0.958	ATATATATATATA=0.000, ATATATATATATATA=0.042, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	0.937238	0.020921	0.041841	32
African Others	Sub	36	ATATATATATATATATA=0.94	ATATATATATATA=0.00, ATATATATATATATA=0.06, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	0.888889	0.0	0.111111	0
African American	Sub	920	ATATATATATATATATA=0.959	ATATATATATATA=0.000, ATATATATATATATA=0.041, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	0.93913	0.021739	0.03913	32
Asian	Sub	18	ATATATATATATATATA=0.89	ATATATATATATA=0.00, ATATATATATATATA=0.11, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	0.777778	0.0	0.222222	0
East Asian	Sub	12	ATATATATATATATATA=0.92	ATATATATATATA=0.00, ATATATATATATATA=0.08, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	0.833333	0.0	0.166667	0
Other Asian	Sub	6	ATATATATATATATATA=0.8	ATATATATATATA=0.0, ATATATATATATATA=0.2, ATATATATATATATATATA=0.0, ATATATATATATATATATATA=0.0, ATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATA=0.0	0.666667	0.0	0.333333	0
Latin American 1	Sub	12	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	80	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	10	ATATATATATATATATA=0.9	ATATATATATATA=0.0, ATATATATATATATA=0.1, ATATATATATATATATATA=0.0, ATATATATATATATATATATA=0.0, ATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATA=0.0	0.8	0.0	0.2	0
Other	Sub	107	ATATATATATATATATA=0.822	ATATATATATATA=0.000, ATATATATATATATA=0.178, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	0.735849	0.075472	0.188679	4

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
TopMed	Global	Study-wide	264690	(AT)₈A=0.415358	delTA=0.584642
Allele Frequency Aggregator	Total	Global	7629	(AT)₈A=0.3924	delTATA=0.0000, delTA=0.5979, dupTA=0.0096, dupTATA=0.0001, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000, dup(TA)₆=0.0000
Allele Frequency Aggregator	European	Sub	6446	(AT)₈A=0.2906	delTATA=0.0000, delTA=0.6980, dupTA=0.0113, dupTATA=0.0002, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000, dup(TA)₆=0.0000
Allele Frequency Aggregator	African	Sub	956	(AT)₈A=0.958	delTATA=0.000, delTA=0.042, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000
Allele Frequency Aggregator	Other	Sub	107	(AT)₈A=0.822	delTATA=0.000, delTA=0.178, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	80	(AT)₈A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00
Allele Frequency Aggregator	Asian	Sub	18	(AT)₈A=0.89	delTATA=0.00, delTA=0.11, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(AT)₈A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(AT)₈A=0.9	delTATA=0.0, delTA=0.1, dupTA=0.0, dupTATA=0.0, dup(TA)₃=0.0, dup(TA)₄=0.0, dup(TA)₅=0.0, dup(TA)₆=0.0
The Danish reference pan genome	Danish	Study-wide	36	(AT)₈A=0.19	delTA=0.81

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 2	NC_000002.12:g.66602265TA[5]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[6]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[7]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[9]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[10]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[11]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[12]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[13]
GRCh38.p14 chr 2	NC_000002.12:g.66602265TA[14]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[5]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[6]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[7]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[9]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[10]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[11]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[12]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[13]
GRCh37.p13 chr 2	NC_000002.11:g.66829397TA[14]

Gene: LINC01798, long intergenic non-protein coding RNA 1798 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01798 transcript	NR_110156.1: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	(AT)₈A=	del(TA)₃	delTATA	delTA	dupTA	dupTATA	dup(TA)₃	dup(TA)₄	dup(TA)₅	dup(TA)₆
GRCh38.p14 chr 2	NC_000002.12:g.66602264_66602280=	NC_000002.12:g.66602265TA[5]	NC_000002.12:g.66602265TA[6]	NC_000002.12:g.66602265TA[7]	NC_000002.12:g.66602265TA[9]	NC_000002.12:g.66602265TA[10]	NC_000002.12:g.66602265TA[11]	NC_000002.12:g.66602265TA[12]	NC_000002.12:g.66602265TA[13]	NC_000002.12:g.66602265TA[14]
GRCh37.p13 chr 2	NC_000002.11:g.66829396_66829412=	NC_000002.11:g.66829397TA[5]	NC_000002.11:g.66829397TA[6]	NC_000002.11:g.66829397TA[7]	NC_000002.11:g.66829397TA[9]	NC_000002.11:g.66829397TA[10]	NC_000002.11:g.66829397TA[11]	NC_000002.11:g.66829397TA[12]	NC_000002.11:g.66829397TA[13]	NC_000002.11:g.66829397TA[14]

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#.

54 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80772568	Jan 10, 2018 (151)
2	HUMANGENOME_JCVI	ss95275381	Feb 04, 2009 (130)
3	GMI	ss288174210	May 04, 2012 (137)
4	PJP	ss294988020	May 09, 2011 (137)
5	PJP	ss294988021	May 09, 2011 (137)
6	1000GENOMES	ss326208324	May 09, 2011 (135)
7	1000GENOMES	ss326220002	May 09, 2011 (135)
8	1000GENOMES	ss326285641	May 09, 2011 (135)
9	LUNTER	ss551089006	Apr 25, 2013 (138)
10	LUNTER	ss551136657	Apr 25, 2013 (138)
11	LUNTER	ss552899900	Apr 25, 2013 (138)
12	SSMP	ss663321761	Apr 01, 2015 (144)
13	DDI	ss1536292012	Apr 01, 2015 (144)
14	EVA_GENOME_DK	ss1575427747	Apr 01, 2015 (144)
15	MCHAISSO	ss3063940151	Nov 08, 2017 (151)
16	MCHAISSO	ss3063940152	Nov 08, 2017 (151)
17	MCHAISSO	ss3064791156	Nov 08, 2017 (151)
18	URBANLAB	ss3647054292	Oct 11, 2018 (152)
19	EVA_DECODE	ss3704088733	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704088734	Jul 13, 2019 (153)
21	EVA_DECODE	ss3704088735	Jul 13, 2019 (153)
22	EVA_DECODE	ss3704088736	Jul 13, 2019 (153)
23	EVA_DECODE	ss3704088737	Jul 13, 2019 (153)
24	PACBIO	ss3783887955	Jul 13, 2019 (153)
25	PACBIO	ss3783887956	Jul 13, 2019 (153)
26	PACBIO	ss3789470766	Jul 13, 2019 (153)
27	PACBIO	ss3789470767	Jul 13, 2019 (153)
28	PACBIO	ss3794343696	Jul 13, 2019 (153)
29	PACBIO	ss3794343697	Jul 13, 2019 (153)
30	EVA	ss3827030229	Apr 25, 2020 (154)
31	EVA	ss3842340615	Apr 25, 2020 (154)
32	KOGIC	ss3947948780	Apr 25, 2020 (154)
33	KOGIC	ss3947948781	Apr 25, 2020 (154)
34	KOGIC	ss3947948782	Apr 25, 2020 (154)
35	GNOMAD	ss4043069489	Apr 26, 2021 (155)
36	GNOMAD	ss4043069490	Apr 26, 2021 (155)
37	GNOMAD	ss4043069491	Apr 26, 2021 (155)
38	GNOMAD	ss4043069492	Apr 26, 2021 (155)
39	GNOMAD	ss4043069493	Apr 26, 2021 (155)
40	GNOMAD	ss4043069494	Apr 26, 2021 (155)
41	GNOMAD	ss4043069496	Apr 26, 2021 (155)
42	GNOMAD	ss4043069497	Apr 26, 2021 (155)
43	TOPMED	ss4509373522	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5151822931	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5151822932	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5248409325	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5448580643	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5448580645	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5680579102	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5680579104	Oct 12, 2022 (156)
51	EVA	ss5820232441	Oct 12, 2022 (156)
52	EVA	ss5820232442	Oct 12, 2022 (156)
53	EVA	ss5820232443	Oct 12, 2022 (156)
54	EVA	ss5930771691	Oct 12, 2022 (156)
55	The Danish reference pan genome	NC_000002.11 - 66829396	Apr 25, 2020 (154)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61140623 (NC_000002.12:66602263::AT 3446/128198) Row 61140624 (NC_000002.12:66602263::ATAT 62/128226) Row 61140625 (NC_000002.12:66602263::ATATAT 1/128232)...	-	Apr 26, 2021 (155)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 4326781 (NC_000002.12:66602267:AT: 1003/1798) Row 4326782 (NC_000002.12:66602265:ATAT: 12/1798) Row 4326783 (NC_000002.12:66602269::AT 1/1798)	-	Apr 25, 2020 (154)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 4326781 (NC_000002.12:66602267:AT: 1003/1798) Row 4326782 (NC_000002.12:66602265:ATAT: 12/1798) Row 4326783 (NC_000002.12:66602269::AT 1/1798)	-	Apr 25, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 4326781 (NC_000002.12:66602267:AT: 1003/1798) Row 4326782 (NC_000002.12:66602265:ATAT: 12/1798) Row 4326783 (NC_000002.12:66602269::AT 1/1798)	-	Apr 25, 2020 (154)
67	8.3KJPN Submission ignored due to conflicting rows: Row 9792238 (NC_000002.11:66829395:AT: 9474/16758) Row 9792239 (NC_000002.11:66829395::AT 1/16758)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 9792238 (NC_000002.11:66829395:AT: 9474/16758) Row 9792239 (NC_000002.11:66829395::AT 1/16758)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 14416206 (NC_000002.12:66602263:AT: 16025/28254) Row 14416208 (NC_000002.12:66602263::AT 1/28254)	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 14416206 (NC_000002.12:66602263:AT: 16025/28254) Row 14416208 (NC_000002.12:66602263::AT 1/28254)	-	Oct 12, 2022 (156)
71	TopMed	NC_000002.12 - 66602264	Apr 26, 2021 (155)
72	ALFA	NC_000002.12 - 66602264	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)
rs72137919	May 11, 2012 (137)
rs141779283	Sep 17, 2011 (135)
rs144663661	Sep 17, 2011 (135)
rs71886657	May 11, 2012 (137)
rs72226355	May 11, 2012 (137)
rs150580466	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3704088737	NC_000002.12:66602263:ATATAT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATA	(self)
ss5820232443	NC_000002.11:66829395:ATAT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA
ss3063940151, ss4043069497	NC_000002.12:66602263:ATAT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA	(self)
ss3704088736, ss3947948781	NC_000002.12:66602265:ATAT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA	(self)
ss80772568	NC_000002.9:66741061:TA:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss288174210, ss326208324, ss326220002, ss326285641, ss551089006, ss551136657, ss552899900	NC_000002.10:66682899:AT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss294988020	NC_000002.10:66682903:AT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss294988021	NC_000002.10:66682910:TA:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
672736, ss663321761, ss1536292012, ss1575427747, ss3783887955, ss3789470766, ss3794343696, ss3827030229, ss5151822931, ss5820232441	NC_000002.11:66829395:AT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
313196401, ss3063940152, ss3064791156, ss3647054292, ss3842340615, ss4043069496, ss4509373522, ss5248409325, ss5448580643, ss5680579102, ss5930771691	NC_000002.12:66602263:AT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss3704088735, ss3947948780	NC_000002.12:66602267:AT:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss95275381	NT_022184.15:45651297:TA:	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA	(self)
ss3783887956, ss3789470767, ss3794343697, ss5151822932, ss5820232442	NC_000002.11:66829395::AT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss4043069489, ss5448580645, ss5680579104	NC_000002.12:66602263::AT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss3704088734, ss3947948782	NC_000002.12:66602269::AT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss4043069490	NC_000002.12:66602263::ATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3704088733	NC_000002.12:66602269::ATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss4043069491	NC_000002.12:66602263::ATATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss4043069492	NC_000002.12:66602263::ATATATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
ss4043069493	NC_000002.12:66602263::ATATATATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)
ss4043069494	NC_000002.12:66602263::ATATATATATAT	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATATA	(self)
10142944730	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATATA	NC_000002.12:66602263:ATATATATATAT… NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATATA	(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 rs10569711

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

rs10569711