Name: rs35333881
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.

rs35333881

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:118958408-118958422 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₉ / dup(A)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0543 (532/9796, ALFA)
delA=0.2079 (1041/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MARCO : 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	9796	AAAAAAAAAAAAAAA=0.8962	AAAAAAAAAAAA=0.0190, AAAAAAAAAAAAA=0.0543, AAAAAAAAAAAAAA=0.0274, AAAAAAAAAAAAAAAA=0.0024, AAAAAAAAAAAAAAAAAAAAAAAA=0.0007, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	0.901393	0.008311	0.090296	28
European	Sub	8370	AAAAAAAAAAAAAAA=0.8787	AAAAAAAAAAAA=0.0222, AAAAAAAAAAAAA=0.0634, AAAAAAAAAAAAAA=0.0319, AAAAAAAAAAAAAAAA=0.0029, AAAAAAAAAAAAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	0.882888	0.009893	0.107219	20
African	Sub	820	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	792	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	74	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	266	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	18	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	222	AAAAAAAAAAAAAAA=0.991	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.005, AAAAAAAAAAAAAA=0.005, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	0.990909	0.0	0.009091	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9796	(A)₁₅=0.8962	delAAA=0.0190, delAA=0.0543, delA=0.0274, dupA=0.0024, dupAA=0.0000, dupAAA=0.0000, dup(A)₉=0.0007
Allele Frequency Aggregator	European	Sub	8370	(A)₁₅=0.8787	delAAA=0.0222, delAA=0.0634, delA=0.0319, dupA=0.0029, dupAA=0.0000, dupAAA=0.0000, dup(A)₉=0.0008
Allele Frequency Aggregator	African	Sub	820	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	266	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Other	Sub	222	(A)₁₅=0.991	delAAA=0.000, delAA=0.005, delA=0.005, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	74	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	Asian	Sub	26	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₉=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.7921	delA=0.2079
1000Genomes	African	Sub	1322	(A)₁₅=0.7474	delA=0.2526
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.8254	delA=0.1746
1000Genomes	Europe	Sub	1006	(A)₁₅=0.8181	delA=0.1819
1000Genomes	South Asian	Sub	978	(A)₁₅=0.757	delA=0.243
1000Genomes	American	Sub	694	(A)₁₅=0.841	delA=0.159

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.118958419_118958422del
GRCh38.p14 chr 2	NC_000002.12:g.118958420_118958422del
GRCh38.p14 chr 2	NC_000002.12:g.118958421_118958422del
GRCh38.p14 chr 2	NC_000002.12:g.118958422del
GRCh38.p14 chr 2	NC_000002.12:g.118958422dup
GRCh38.p14 chr 2	NC_000002.12:g.118958421_118958422dup
GRCh38.p14 chr 2	NC_000002.12:g.118958420_118958422dup
GRCh38.p14 chr 2	NC_000002.12:g.118958419_118958422dup
GRCh38.p14 chr 2	NC_000002.12:g.118958414_118958422dup
GRCh38.p14 chr 2	NC_000002.12:g.118958413_118958422dup
GRCh37.p13 chr 2	NC_000002.11:g.119715995_119715998del
GRCh37.p13 chr 2	NC_000002.11:g.119715996_119715998del
GRCh37.p13 chr 2	NC_000002.11:g.119715997_119715998del
GRCh37.p13 chr 2	NC_000002.11:g.119715998del
GRCh37.p13 chr 2	NC_000002.11:g.119715998dup
GRCh37.p13 chr 2	NC_000002.11:g.119715997_119715998dup
GRCh37.p13 chr 2	NC_000002.11:g.119715996_119715998dup
GRCh37.p13 chr 2	NC_000002.11:g.119715995_119715998dup
GRCh37.p13 chr 2	NC_000002.11:g.119715990_119715998dup
GRCh37.p13 chr 2	NC_000002.11:g.119715989_119715998dup

Gene: MARCO, macrophage receptor with collagenous structure (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MARCO transcript	NM_006770.4:c.98-10741_98… NM_006770.4:c.98-10741_98-10738del	N/A	Intron Variant
MARCO transcript variant X1	XM_011512082.3:c.98-10741… XM_011512082.3:c.98-10741_98-10738del	N/A	Intron Variant
MARCO transcript variant X2	XM_011512083.4:c.98-15914… XM_011512083.4:c.98-15914_98-15911del	N/A	Intron Variant
MARCO transcript variant X3	XM_017005171.3:c.98-10741… XM_017005171.3:c.98-10741_98-10738del	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)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₉	dup(A)₁₀
GRCh38.p14 chr 2	NC_000002.12:g.118958408_118958422=	NC_000002.12:g.118958419_118958422del	NC_000002.12:g.118958420_118958422del	NC_000002.12:g.118958421_118958422del	NC_000002.12:g.118958422del	NC_000002.12:g.118958422dup	NC_000002.12:g.118958421_118958422dup	NC_000002.12:g.118958420_118958422dup	NC_000002.12:g.118958419_118958422dup	NC_000002.12:g.118958414_118958422dup	NC_000002.12:g.118958413_118958422dup
GRCh37.p13 chr 2	NC_000002.11:g.119715984_119715998=	NC_000002.11:g.119715995_119715998del	NC_000002.11:g.119715996_119715998del	NC_000002.11:g.119715997_119715998del	NC_000002.11:g.119715998del	NC_000002.11:g.119715998dup	NC_000002.11:g.119715997_119715998dup	NC_000002.11:g.119715996_119715998dup	NC_000002.11:g.119715995_119715998dup	NC_000002.11:g.119715990_119715998dup	NC_000002.11:g.119715989_119715998dup
MARCO transcript	NM_006770.3:c.98-10752=	NM_006770.3:c.98-10741_98-10738del	NM_006770.3:c.98-10740_98-10738del	NM_006770.3:c.98-10739_98-10738del	NM_006770.3:c.98-10738del	NM_006770.3:c.98-10738dup	NM_006770.3:c.98-10739_98-10738dup	NM_006770.3:c.98-10740_98-10738dup	NM_006770.3:c.98-10741_98-10738dup	NM_006770.3:c.98-10746_98-10738dup	NM_006770.3:c.98-10747_98-10738dup
MARCO transcript	NM_006770.4:c.98-10752=	NM_006770.4:c.98-10741_98-10738del	NM_006770.4:c.98-10740_98-10738del	NM_006770.4:c.98-10739_98-10738del	NM_006770.4:c.98-10738del	NM_006770.4:c.98-10738dup	NM_006770.4:c.98-10739_98-10738dup	NM_006770.4:c.98-10740_98-10738dup	NM_006770.4:c.98-10741_98-10738dup	NM_006770.4:c.98-10746_98-10738dup	NM_006770.4:c.98-10747_98-10738dup
MARCO transcript variant X1	XM_011512082.3:c.98-10752=	XM_011512082.3:c.98-10741_98-10738del	XM_011512082.3:c.98-10740_98-10738del	XM_011512082.3:c.98-10739_98-10738del	XM_011512082.3:c.98-10738del	XM_011512082.3:c.98-10738dup	XM_011512082.3:c.98-10739_98-10738dup	XM_011512082.3:c.98-10740_98-10738dup	XM_011512082.3:c.98-10741_98-10738dup	XM_011512082.3:c.98-10746_98-10738dup	XM_011512082.3:c.98-10747_98-10738dup
MARCO transcript variant X2	XM_011512083.4:c.98-15925=	XM_011512083.4:c.98-15914_98-15911del	XM_011512083.4:c.98-15913_98-15911del	XM_011512083.4:c.98-15912_98-15911del	XM_011512083.4:c.98-15911del	XM_011512083.4:c.98-15911dup	XM_011512083.4:c.98-15912_98-15911dup	XM_011512083.4:c.98-15913_98-15911dup	XM_011512083.4:c.98-15914_98-15911dup	XM_011512083.4:c.98-15919_98-15911dup	XM_011512083.4:c.98-15920_98-15911dup
MARCO transcript variant X3	XM_017005171.3:c.98-10752=	XM_017005171.3:c.98-10741_98-10738del	XM_017005171.3:c.98-10740_98-10738del	XM_017005171.3:c.98-10739_98-10738del	XM_017005171.3:c.98-10738del	XM_017005171.3:c.98-10738dup	XM_017005171.3:c.98-10739_98-10738dup	XM_017005171.3:c.98-10740_98-10738dup	XM_017005171.3:c.98-10741_98-10738dup	XM_017005171.3:c.98-10746_98-10738dup	XM_017005171.3:c.98-10747_98-10738dup

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, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41831235	Mar 15, 2016 (147)
2	HUMANGENOME_JCVI	ss95282770	Oct 11, 2018 (152)
3	HUMANGENOME_JCVI	ss96728343	Oct 11, 2018 (152)
4	GMI	ss287704240	Mar 15, 2016 (147)
5	GMI	ss288210157	May 04, 2012 (137)
6	GMI	ss288210159	May 04, 2012 (137)
7	PJP	ss294999535	May 09, 2011 (137)
8	SSMP	ss663228929	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666162025	Apr 25, 2013 (138)
10	1000GENOMES	ss1368670714	Aug 21, 2014 (142)
11	DDI	ss1536303520	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1703047897	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1703048008	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1710021178	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710021183	Apr 01, 2015 (144)
16	SWEGEN	ss2990270906	Nov 08, 2017 (151)
17	URBANLAB	ss3647124193	Oct 11, 2018 (152)
18	EVA_DECODE	ss3704725405	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704725406	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704725407	Jul 13, 2019 (153)
21	EVA_DECODE	ss3704725408	Jul 13, 2019 (153)
22	ACPOP	ss3728793747	Jul 13, 2019 (153)
23	ACPOP	ss3728793748	Jul 13, 2019 (153)
24	ACPOP	ss3728793749	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3801641421	Jul 13, 2019 (153)
26	EVA	ss3827177654	Apr 25, 2020 (154)
27	GNOMAD	ss4049253293	Apr 26, 2021 (155)
28	GNOMAD	ss4049253294	Apr 26, 2021 (155)
29	GNOMAD	ss4049253295	Apr 26, 2021 (155)
30	GNOMAD	ss4049253296	Apr 26, 2021 (155)
31	GNOMAD	ss4049253297	Apr 26, 2021 (155)
32	GNOMAD	ss4049253298	Apr 26, 2021 (155)
33	GNOMAD	ss4049253299	Apr 26, 2021 (155)
34	GNOMAD	ss4049253300	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5153456921	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5153456922	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5153456923	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5153456924	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5153456925	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5249694483	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5249694484	Oct 12, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5249694485	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5249694486	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5449563498	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5449563499	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5449563500	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5449563501	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5683458075	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5683458076	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5683458077	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5683458078	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5683458079	Oct 12, 2022 (156)
53	EVA	ss5820681126	Oct 12, 2022 (156)
54	EVA	ss5820681127	Oct 12, 2022 (156)
55	1000Genomes	NC_000002.11 - 119715984	Oct 11, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5504671 (NC_000002.11:119715984:A: 511/3854) Row 5504672 (NC_000002.11:119715983:AAA: 199/3854)	-	Oct 11, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5504671 (NC_000002.11:119715984:A: 511/3854) Row 5504672 (NC_000002.11:119715983:AAA: 199/3854)	-	Oct 11, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71237835 (NC_000002.12:118958407::A 1924/116872) Row 71237836 (NC_000002.12:118958407::AA 10/116928) Row 71237837 (NC_000002.12:118958407::AAAA 1/116930)...	-	Apr 26, 2021 (155)
66	Northern Sweden Submission ignored due to conflicting rows: Row 2078612 (NC_000002.11:119715983:AAA: 39/578) Row 2078613 (NC_000002.11:119715983:A: 51/578) Row 2078614 (NC_000002.11:119715983:AA: 70/578)	-	Jul 13, 2019 (153)
67	Northern Sweden Submission ignored due to conflicting rows: Row 2078612 (NC_000002.11:119715983:AAA: 39/578) Row 2078613 (NC_000002.11:119715983:A: 51/578) Row 2078614 (NC_000002.11:119715983:AA: 70/578)	-	Jul 13, 2019 (153)
68	Northern Sweden Submission ignored due to conflicting rows: Row 2078612 (NC_000002.11:119715983:AAA: 39/578) Row 2078613 (NC_000002.11:119715983:A: 51/578) Row 2078614 (NC_000002.11:119715983:AA: 70/578)	-	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 11426228 (NC_000002.11:119715983:AA: 5200/16760) Row 11426229 (NC_000002.11:119715983::A 237/16760) Row 11426230 (NC_000002.11:119715983:A: 1611/16760)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 11426228 (NC_000002.11:119715983:AA: 5200/16760) Row 11426229 (NC_000002.11:119715983::A 237/16760) Row 11426230 (NC_000002.11:119715983:A: 1611/16760)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 11426228 (NC_000002.11:119715983:AA: 5200/16760) Row 11426229 (NC_000002.11:119715983::A 237/16760) Row 11426230 (NC_000002.11:119715983:A: 1611/16760)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 11426228 (NC_000002.11:119715983:AA: 5200/16760) Row 11426229 (NC_000002.11:119715983::A 237/16760) Row 11426230 (NC_000002.11:119715983:A: 1611/16760)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 11426228 (NC_000002.11:119715983:AA: 5200/16760) Row 11426229 (NC_000002.11:119715983::A 237/16760) Row 11426230 (NC_000002.11:119715983:A: 1611/16760)...	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 17295179 (NC_000002.12:118958407:AA: 8770/28252) Row 17295180 (NC_000002.12:118958407:A: 2720/28252) Row 17295181 (NC_000002.12:118958407::A 420/28252)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 17295179 (NC_000002.12:118958407:AA: 8770/28252) Row 17295180 (NC_000002.12:118958407:A: 2720/28252) Row 17295181 (NC_000002.12:118958407::A 420/28252)...	-	Oct 12, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 17295179 (NC_000002.12:118958407:AA: 8770/28252) Row 17295180 (NC_000002.12:118958407:A: 2720/28252) Row 17295181 (NC_000002.12:118958407::A 420/28252)...	-	Oct 12, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 17295179 (NC_000002.12:118958407:AA: 8770/28252) Row 17295180 (NC_000002.12:118958407:A: 2720/28252) Row 17295181 (NC_000002.12:118958407::A 420/28252)...	-	Oct 12, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 17295179 (NC_000002.12:118958407:AA: 8770/28252) Row 17295180 (NC_000002.12:118958407:A: 2720/28252) Row 17295181 (NC_000002.12:118958407::A 420/28252)...	-	Oct 12, 2022 (156)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5504671 (NC_000002.11:119715984:A: 516/3708) Row 5504672 (NC_000002.11:119715983:AAA: 199/3708)	-	Oct 11, 2018 (152)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5504671 (NC_000002.11:119715984:A: 516/3708) Row 5504672 (NC_000002.11:119715983:AAA: 199/3708)	-	Oct 11, 2018 (152)
81	ALFA	NC_000002.12 - 118958408	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)
rs68004047	Feb 27, 2009 (130)
rs149116546	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4049253300	NC_000002.12:118958407:AAAA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss294999535	NC_000002.10:119432453:AAA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1703047897, ss1703048008, ss2990270906, ss3728793747, ss5153456924, ss5820681127	NC_000002.11:119715983:AAA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3647124193, ss3704725408, ss4049253299, ss5249694486, ss5449563500, ss5683458078	NC_000002.12:118958407:AAA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss288210159	NC_000002.10:119432453:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss663228929, ss1536303520, ss3728793749, ss5153456921, ss5820681126	NC_000002.11:119715983:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710021178, ss1710021183	NC_000002.11:119715984:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4049253298, ss5249694483, ss5449563498, ss5683458075	NC_000002.12:118958407:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3704725407	NC_000002.12:118958408:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss41831235, ss287704240	NT_022135.16:9464646:AA:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288210157	NC_000002.10:119432453:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9973686, ss666162025, ss1368670714, ss3728793748, ss3827177654, ss5153456923	NC_000002.11:119715983:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
	NC_000002.11:119715984:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3801641421, ss4049253297, ss5249694484, ss5449563499, ss5683458076	NC_000002.12:118958407:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3704725406	NC_000002.12:118958409:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95282770, ss96728343	NT_022135.16:9464660:A:	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5153456922	NC_000002.11:119715983::A	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4049253293, ss5249694485, ss5449563501, ss5683458077	NC_000002.12:118958407::A	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3704725405	NC_000002.12:118958410::A	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5153456925	NC_000002.11:119715983::AA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4049253294, ss5683458079	NC_000002.12:118958407::AA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95282770, ss96728343	NT_022135.16:9464660:A:AAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4049253295	NC_000002.12:118958407::AAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4732116316	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4049253296	NC_000002.12:118958407::AAAAAAAAAA	NC_000002.12:118958407:AAAAAAAAAAA… NC_000002.12:118958407:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35333881

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

rs35333881