Name: rs35578082
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.

rs35578082

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:19075447-19075459 (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: delAA / delA / dupA / dupAA / dupA…
delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.01565 (243/15532, ALFA)
delA=0.0010 (4/4124, 1000G)
dupA=0.059 (35/594, NorthernSweden) (+ 1 more)
dupA=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DGCR2 : 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	15532	AAAAAAAAAAAAA=0.98435	AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.01565, AAAAAAAAAAAAAAA=0.00000	0.970603	0.001934	0.027463	32
European	Sub	13070	AAAAAAAAAAAAA=0.98148	AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.01852, AAAAAAAAAAAAAAA=0.00000	0.965211	0.002299	0.03249	32
African	Sub	1446	AAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	64	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1382	AAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	56	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	90	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	430	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	360	AAAAAAAAAAAAA=0.997	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAA=0.000	0.994444	0.0	0.005556	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	15532	(A)₁₃=0.98435	delAA=0.00000, delA=0.00000, dupA=0.01565, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	13070	(A)₁₃=0.98148	delAA=0.00000, delA=0.00000, dupA=0.01852, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	1446	(A)₁₃=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	430	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	360	(A)₁₃=0.997	delAA=0.000, delA=0.000, dupA=0.003, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	90	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	80	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	56	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	4124	(A)₁₃=0.9990	delA=0.0010
1000Genomes	African	Sub	957	(A)₁₃=0.996	delA=0.004
1000Genomes	Europe	Sub	931	(A)₁₃=1.000	delA=0.000
1000Genomes	East Asian	Sub	831	(A)₁₃=1.000	delA=0.000
1000Genomes	South Asian	Sub	819	(A)₁₃=1.000	delA=0.000
1000Genomes	American	Sub	586	(A)₁₃=1.000	delA=0.000
Northern Sweden	ACPOP	Study-wide	594	- No frequency provided	dupA=0.059
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.07

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 22	NC_000022.11:g.19075458_19075459del
GRCh38.p14 chr 22	NC_000022.11:g.19075459del
GRCh38.p14 chr 22	NC_000022.11:g.19075459dup
GRCh38.p14 chr 22	NC_000022.11:g.19075458_19075459dup
GRCh38.p14 chr 22	NC_000022.11:g.19075457_19075459dup
GRCh37.p13 chr 22	NC_000022.10:g.19062971_19062972del
GRCh37.p13 chr 22	NC_000022.10:g.19062972del
GRCh37.p13 chr 22	NC_000022.10:g.19062972dup
GRCh37.p13 chr 22	NC_000022.10:g.19062971_19062972dup
GRCh37.p13 chr 22	NC_000022.10:g.19062970_19062972dup
DGCR2 RefSeqGene	NG_021333.2:g.52007_52008del
DGCR2 RefSeqGene	NG_021333.2:g.52008del
DGCR2 RefSeqGene	NG_021333.2:g.52008dup
DGCR2 RefSeqGene	NG_021333.2:g.52007_52008dup
DGCR2 RefSeqGene	NG_021333.2:g.52006_52008dup

Gene: DGCR2, DiGeorge syndrome critical region gene 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DGCR2 transcript variant 2	NM_001173533.2:c.80-7223_… NM_001173533.2:c.80-7223_80-7222del	N/A	Intron Variant
DGCR2 transcript variant 3	NM_001173534.2:c.80-7223_… NM_001173534.2:c.80-7223_80-7222del	N/A	Intron Variant
DGCR2 transcript variant 4	NM_001184781.2:c.203-7223… NM_001184781.2:c.203-7223_203-7222del	N/A	Intron Variant
DGCR2 transcript variant 1	NM_005137.3:c.203-7223_20… NM_005137.3:c.203-7223_203-7222del	N/A	Intron Variant
DGCR2 transcript variant 5	NR_033674.2: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)₁₃=	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 22	NC_000022.11:g.19075447_19075459=	NC_000022.11:g.19075458_19075459del	NC_000022.11:g.19075459del	NC_000022.11:g.19075459dup	NC_000022.11:g.19075458_19075459dup	NC_000022.11:g.19075457_19075459dup
GRCh37.p13 chr 22	NC_000022.10:g.19062960_19062972=	NC_000022.10:g.19062971_19062972del	NC_000022.10:g.19062972del	NC_000022.10:g.19062972dup	NC_000022.10:g.19062971_19062972dup	NC_000022.10:g.19062970_19062972dup
DGCR2 RefSeqGene	NG_021333.2:g.51996_52008=	NG_021333.2:g.52007_52008del	NG_021333.2:g.52008del	NG_021333.2:g.52008dup	NG_021333.2:g.52007_52008dup	NG_021333.2:g.52006_52008dup
DGCR2 transcript variant 2	NM_001173533.1:c.80-7222=	NM_001173533.1:c.80-7223_80-7222del	NM_001173533.1:c.80-7222del	NM_001173533.1:c.80-7222dup	NM_001173533.1:c.80-7223_80-7222dup	NM_001173533.1:c.80-7224_80-7222dup
DGCR2 transcript variant 2	NM_001173533.2:c.80-7222=	NM_001173533.2:c.80-7223_80-7222del	NM_001173533.2:c.80-7222del	NM_001173533.2:c.80-7222dup	NM_001173533.2:c.80-7223_80-7222dup	NM_001173533.2:c.80-7224_80-7222dup
DGCR2 transcript variant 3	NM_001173534.1:c.80-7222=	NM_001173534.1:c.80-7223_80-7222del	NM_001173534.1:c.80-7222del	NM_001173534.1:c.80-7222dup	NM_001173534.1:c.80-7223_80-7222dup	NM_001173534.1:c.80-7224_80-7222dup
DGCR2 transcript variant 3	NM_001173534.2:c.80-7222=	NM_001173534.2:c.80-7223_80-7222del	NM_001173534.2:c.80-7222del	NM_001173534.2:c.80-7222dup	NM_001173534.2:c.80-7223_80-7222dup	NM_001173534.2:c.80-7224_80-7222dup
DGCR2 transcript variant 4	NM_001184781.1:c.203-7222=	NM_001184781.1:c.203-7223_203-7222del	NM_001184781.1:c.203-7222del	NM_001184781.1:c.203-7222dup	NM_001184781.1:c.203-7223_203-7222dup	NM_001184781.1:c.203-7224_203-7222dup
DGCR2 transcript variant 4	NM_001184781.2:c.203-7222=	NM_001184781.2:c.203-7223_203-7222del	NM_001184781.2:c.203-7222del	NM_001184781.2:c.203-7222dup	NM_001184781.2:c.203-7223_203-7222dup	NM_001184781.2:c.203-7224_203-7222dup
DGCR2 transcript variant 1	NM_005137.2:c.203-7222=	NM_005137.2:c.203-7223_203-7222del	NM_005137.2:c.203-7222del	NM_005137.2:c.203-7222dup	NM_005137.2:c.203-7223_203-7222dup	NM_005137.2:c.203-7224_203-7222dup
DGCR2 transcript variant 1	NM_005137.3:c.203-7222=	NM_005137.3:c.203-7223_203-7222del	NM_005137.3:c.203-7222del	NM_005137.3:c.203-7222dup	NM_005137.3:c.203-7223_203-7222dup	NM_005137.3:c.203-7224_203-7222dup

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#.

33 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41521621	Mar 15, 2006 (126)
2	HGSV	ss82681068	Dec 15, 2007 (130)
3	HGSV	ss83749049	Dec 15, 2007 (130)
4	SSMP	ss664515874	Apr 01, 2015 (144)
5	SSIP	ss947414013	Aug 21, 2014 (142)
6	1000GENOMES	ss1378891921	Aug 21, 2014 (142)
7	1000GENOMES	ss1378891925	Aug 21, 2014 (142)
8	EVA_GENOME_DK	ss1575806194	Apr 01, 2015 (144)
9	HAMMER_LAB	ss1809730856	Sep 08, 2015 (146)
10	SYSTEMSBIOZJU	ss2629578675	Nov 08, 2017 (151)
11	SWEGEN	ss3019074528	Nov 08, 2017 (151)
12	MCHAISSO	ss3065848929	Nov 08, 2017 (151)
13	ACPOP	ss3743816967	Jul 13, 2019 (153)
14	PACBIO	ss3788791407	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3822390348	Jul 13, 2019 (153)
16	EVA	ss3835923969	Apr 27, 2020 (154)
17	KOGIC	ss3983374253	Apr 27, 2020 (154)
18	KOGIC	ss3983374254	Apr 27, 2020 (154)
19	GNOMAD	ss4362436917	Apr 27, 2021 (155)
20	GNOMAD	ss4362436918	Apr 27, 2021 (155)
21	GNOMAD	ss4362436919	Apr 27, 2021 (155)
22	GNOMAD	ss4362436920	Apr 27, 2021 (155)
23	GNOMAD	ss4362436921	Apr 27, 2021 (155)
24	TOMMO_GENOMICS	ss5232008622	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5232008623	Apr 27, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5310633960	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5310633961	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5310633962	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5502547554	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5502547555	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5792949121	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5792949122	Oct 16, 2022 (156)
33	EVA	ss5853343278	Oct 16, 2022 (156)
34	1000Genomes	NC_000022.10 - 19062960	Oct 12, 2018 (152)
35	The Danish reference pan genome	NC_000022.10 - 19062960	Apr 27, 2020 (154)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566352266 (NC_000022.11:19075446::A 20296/125086) Row 566352267 (NC_000022.11:19075446::AA 24/125304) Row 566352268 (NC_000022.11:19075446::AAA 1/125312)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566352266 (NC_000022.11:19075446::A 20296/125086) Row 566352267 (NC_000022.11:19075446::AA 24/125304) Row 566352268 (NC_000022.11:19075446::AAA 1/125312)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566352266 (NC_000022.11:19075446::A 20296/125086) Row 566352267 (NC_000022.11:19075446::AA 24/125304) Row 566352268 (NC_000022.11:19075446::AAA 1/125312)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566352266 (NC_000022.11:19075446::A 20296/125086) Row 566352267 (NC_000022.11:19075446::AA 24/125304) Row 566352268 (NC_000022.11:19075446::AAA 1/125312)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566352266 (NC_000022.11:19075446::A 20296/125086) Row 566352267 (NC_000022.11:19075446::AA 24/125304) Row 566352268 (NC_000022.11:19075446::AAA 1/125312)...	-	Apr 27, 2021 (155)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 39752254 (NC_000022.11:19075447::A 348/1832) Row 39752255 (NC_000022.11:19075446:A: 47/1832)	-	Apr 27, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 39752254 (NC_000022.11:19075447::A 348/1832) Row 39752255 (NC_000022.11:19075446:A: 47/1832)	-	Apr 27, 2020 (154)
43	Northern Sweden	NC_000022.10 - 19062960	Jul 13, 2019 (153)
44	8.3KJPN Submission ignored due to conflicting rows: Row 89977929 (NC_000022.10:19062959::A 3160/16758) Row 89977930 (NC_000022.10:19062959::AA 3/16758)	-	Apr 27, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 89977929 (NC_000022.10:19062959::A 3160/16758) Row 89977930 (NC_000022.10:19062959::AA 3/16758)	-	Apr 27, 2021 (155)
46	14KJPN Submission ignored due to conflicting rows: Row 126786225 (NC_000022.11:19075446::A 5448/28258) Row 126786226 (NC_000022.11:19075446::AA 2/28258)	-	Oct 16, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 126786225 (NC_000022.11:19075446::A 5448/28258) Row 126786226 (NC_000022.11:19075446::AA 2/28258)	-	Oct 16, 2022 (156)
48	ALFA	NC_000022.11 - 19075447	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)
rs59727996	May 26, 2008 (130)
rs919701736	Nov 08, 2017 (151)
rs974105320	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4362436921	NC_000022.11:19075446:AA:	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
17089937530	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
80189269, ss1378891921, ss3788791407	NC_000022.10:19062959:A:	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3983374254, ss4362436920, ss5310633961	NC_000022.11:19075446:A:	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
17089937530	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
787787, 17101832, ss664515874, ss1575806194, ss1809730856, ss2629578675, ss3019074528, ss3743816967, ss3835923969, ss5232008622	NC_000022.10:19062959::A	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss947414013, ss1378891925	NC_000022.10:19062960::A	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3065848929, ss4362436917, ss5310633960, ss5502547554, ss5792949121, ss5853343278	NC_000022.11:19075446::A	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
17089937530	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3822390348, ss3983374253	NC_000022.11:19075447::A	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss41521621, ss83749049	NT_011519.10:2215122::A	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5232008623	NC_000022.10:19062959::AA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4362436918, ss5310633962, ss5502547555, ss5792949122	NC_000022.11:19075446::AA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
17089937530	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss82681068	NT_011519.10:2215122::AA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4362436919	NC_000022.11:19075446::AAA	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2413225689	NC_000022.10:19062959:AA:	NC_000022.11:19075446:AAAAAAAAAAAA… NC_000022.11:19075446:AAAAAAAAAAAAA:AAAAAAAAAAA

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

No publications for rs35578082

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

rs35578082