Name: rs28360426
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.

rs28360426

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:171283311-171283319 (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 / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/7282, ALFA)
delA=0.0000 (0/7282, ALFA)
dupA=0.0000 (0/7282, ALFA) (+ 5 more)
dupAA=0.0000 (0/7282, ALFA)
dupAAA=0.0000 (0/7282, ALFA)
dup(A)₅=0.0000 (0/7282, ALFA)
dupA=0.094 (54/574, NorthernSweden)
dupA=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FMO1 : 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	HWEP
Total	Global	7282	AAAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	5700	AAAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	506	AAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	22	AAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	484	AAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	102	AAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	78	AAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	100	AAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	522	AAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	64	AAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	288	AAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	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	7282	(A)₉=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	5700	(A)₉=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	522	(A)₉=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	506	(A)₉=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	288	(A)₉=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Asian	Sub	102	(A)₉=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(A)₉=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	64	(A)₉=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Northern Sweden	ACPOP	Study-wide	574	- No frequency provided	dupA=0.094
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.17

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.171283318_171283319del
GRCh38.p14 chr 1	NC_000001.11:g.171283319del
GRCh38.p14 chr 1	NC_000001.11:g.171283319dup
GRCh38.p14 chr 1	NC_000001.11:g.171283318_171283319dup
GRCh38.p14 chr 1	NC_000001.11:g.171283317_171283319dup
GRCh38.p14 chr 1	NC_000001.11:g.171283315_171283319dup
GRCh37.p13 chr 1	NC_000001.10:g.171252457_171252458del
GRCh37.p13 chr 1	NC_000001.10:g.171252458del
GRCh37.p13 chr 1	NC_000001.10:g.171252458dup
GRCh37.p13 chr 1	NC_000001.10:g.171252457_171252458dup
GRCh37.p13 chr 1	NC_000001.10:g.171252456_171252458dup
GRCh37.p13 chr 1	NC_000001.10:g.171252454_171252458dup

Gene: FMO1, flavin containing dimethylaniline monoxygenase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FMO1 transcript variant 1	NM_001282692.1:c.1268+102… NM_001282692.1:c.1268+102_1268+103del	N/A	Intron Variant
FMO1 transcript variant 3	NM_001282693.2:c.1256+102… NM_001282693.2:c.1256+102_1256+103del	N/A	Intron Variant
FMO1 transcript variant 4	NM_001282694.2:c.1067+102… NM_001282694.2:c.1067+102_1067+103del	N/A	Intron Variant
FMO1 transcript variant 2	NM_002021.3:c.1256+102_12… NM_002021.3:c.1256+102_1256+103del	N/A	Intron Variant
FMO1 transcript variant X2	XM_005245037.4:c.968+102_… XM_005245037.4:c.968+102_968+103del	N/A	Intron Variant
FMO1 transcript variant X4	XM_005245038.5:c.1183+985… XM_005245038.5:c.1183+985_1183+986del	N/A	Intron Variant
FMO1 transcript variant X1	XM_006711241.5:c.1151+102… XM_006711241.5:c.1151+102_1151+103del	N/A	Intron Variant
FMO1 transcript variant X3	XM_006711242.5:c.1256+102… XM_006711242.5:c.1256+102_1256+103del	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)₉=	delAA	delA	dupA	dupAA	dupAAA	dup(A)₅
GRCh38.p14 chr 1	NC_000001.11:g.171283311_171283319=	NC_000001.11:g.171283318_171283319del	NC_000001.11:g.171283319del	NC_000001.11:g.171283319dup	NC_000001.11:g.171283318_171283319dup	NC_000001.11:g.171283317_171283319dup	NC_000001.11:g.171283315_171283319dup
GRCh37.p13 chr 1	NC_000001.10:g.171252450_171252458=	NC_000001.10:g.171252457_171252458del	NC_000001.10:g.171252458del	NC_000001.10:g.171252458dup	NC_000001.10:g.171252457_171252458dup	NC_000001.10:g.171252456_171252458dup	NC_000001.10:g.171252454_171252458dup
FMO1 transcript variant 1	NM_001282692.1:c.1268+95=	NM_001282692.1:c.1268+102_1268+103del	NM_001282692.1:c.1268+103del	NM_001282692.1:c.1268+103dup	NM_001282692.1:c.1268+102_1268+103dup	NM_001282692.1:c.1268+101_1268+103dup	NM_001282692.1:c.1268+99_1268+103dup
FMO1 transcript variant 3	NM_001282693.2:c.1256+95=	NM_001282693.2:c.1256+102_1256+103del	NM_001282693.2:c.1256+103del	NM_001282693.2:c.1256+103dup	NM_001282693.2:c.1256+102_1256+103dup	NM_001282693.2:c.1256+101_1256+103dup	NM_001282693.2:c.1256+99_1256+103dup
FMO1 transcript variant 4	NM_001282694.2:c.1067+95=	NM_001282694.2:c.1067+102_1067+103del	NM_001282694.2:c.1067+103del	NM_001282694.2:c.1067+103dup	NM_001282694.2:c.1067+102_1067+103dup	NM_001282694.2:c.1067+101_1067+103dup	NM_001282694.2:c.1067+99_1067+103dup
FMO1 transcript	NM_002021.1:c.1256+95=	NM_002021.1:c.1256+102_1256+103del	NM_002021.1:c.1256+103del	NM_002021.1:c.1256+103dup	NM_002021.1:c.1256+102_1256+103dup	NM_002021.1:c.1256+101_1256+103dup	NM_002021.1:c.1256+99_1256+103dup
FMO1 transcript variant 2	NM_002021.3:c.1256+95=	NM_002021.3:c.1256+102_1256+103del	NM_002021.3:c.1256+103del	NM_002021.3:c.1256+103dup	NM_002021.3:c.1256+102_1256+103dup	NM_002021.3:c.1256+101_1256+103dup	NM_002021.3:c.1256+99_1256+103dup
FMO1 transcript variant X1	XM_005245034.1:c.1256+95=	XM_005245034.1:c.1256+102_1256+103del	XM_005245034.1:c.1256+103del	XM_005245034.1:c.1256+103dup	XM_005245034.1:c.1256+102_1256+103dup	XM_005245034.1:c.1256+101_1256+103dup	XM_005245034.1:c.1256+99_1256+103dup
FMO1 transcript variant X2	XM_005245035.1:c.1067+95=	XM_005245035.1:c.1067+102_1067+103del	XM_005245035.1:c.1067+103del	XM_005245035.1:c.1067+103dup	XM_005245035.1:c.1067+102_1067+103dup	XM_005245035.1:c.1067+101_1067+103dup	XM_005245035.1:c.1067+99_1067+103dup
FMO1 transcript variant X3	XM_005245036.1:c.971+95=	XM_005245036.1:c.971+102_971+103del	XM_005245036.1:c.971+103del	XM_005245036.1:c.971+103dup	XM_005245036.1:c.971+102_971+103dup	XM_005245036.1:c.971+101_971+103dup	XM_005245036.1:c.971+99_971+103dup
FMO1 transcript variant X4	XM_005245037.1:c.968+95=	XM_005245037.1:c.968+102_968+103del	XM_005245037.1:c.968+103del	XM_005245037.1:c.968+103dup	XM_005245037.1:c.968+102_968+103dup	XM_005245037.1:c.968+101_968+103dup	XM_005245037.1:c.968+99_968+103dup
FMO1 transcript variant X2	XM_005245037.4:c.968+95=	XM_005245037.4:c.968+102_968+103del	XM_005245037.4:c.968+103del	XM_005245037.4:c.968+103dup	XM_005245037.4:c.968+102_968+103dup	XM_005245037.4:c.968+101_968+103dup	XM_005245037.4:c.968+99_968+103dup
FMO1 transcript variant X5	XM_005245038.1:c.1183+978=	XM_005245038.1:c.1183+985_1183+986del	XM_005245038.1:c.1183+986del	XM_005245038.1:c.1183+986dup	XM_005245038.1:c.1183+985_1183+986dup	XM_005245038.1:c.1183+984_1183+986dup	XM_005245038.1:c.1183+982_1183+986dup
FMO1 transcript variant X4	XM_005245038.5:c.1183+978=	XM_005245038.5:c.1183+985_1183+986del	XM_005245038.5:c.1183+986del	XM_005245038.5:c.1183+986dup	XM_005245038.5:c.1183+985_1183+986dup	XM_005245038.5:c.1183+984_1183+986dup	XM_005245038.5:c.1183+982_1183+986dup
FMO1 transcript variant X1	XM_006711241.5:c.1151+95=	XM_006711241.5:c.1151+102_1151+103del	XM_006711241.5:c.1151+103del	XM_006711241.5:c.1151+103dup	XM_006711241.5:c.1151+102_1151+103dup	XM_006711241.5:c.1151+101_1151+103dup	XM_006711241.5:c.1151+99_1151+103dup
FMO1 transcript variant X3	XM_006711242.5:c.1256+95=	XM_006711242.5:c.1256+102_1256+103del	XM_006711242.5:c.1256+103del	XM_006711242.5:c.1256+103dup	XM_006711242.5:c.1256+102_1256+103dup	XM_006711242.5:c.1256+101_1256+103dup	XM_006711242.5:c.1256+99_1256+103dup

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#.

38 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EGP_SNPS	ss32479826	Dec 03, 2013 (138)
2	HGSV	ss77944025	Dec 06, 2007 (138)
3	HGSV	ss82893350	Dec 15, 2007 (130)
4	BUSHMAN	ss193135588	Jul 04, 2010 (138)
5	GMI	ss287683097	May 09, 2011 (138)
6	1000GENOMES	ss326134375	May 09, 2011 (138)
7	1000GENOMES	ss499033581	May 04, 2012 (138)
8	LUNTER	ss551013040	Apr 25, 2013 (138)
9	SSMP	ss663131785	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666115758	Apr 25, 2013 (138)
11	EVA_GENOME_DK	ss1574048480	Apr 01, 2015 (144)
12	HAMMER_LAB	ss1795263333	Sep 08, 2015 (146)
13	AFFY	ss2985530708	Nov 08, 2017 (151)
14	MCHAISSO	ss3065334622	Nov 08, 2017 (151)
15	BIOINF_KMB_FNS_UNIBA	ss3645079607	Oct 11, 2018 (152)
16	EVA_DECODE	ss3688013465	Jul 12, 2019 (153)
17	ACPOP	ss3727590813	Jul 12, 2019 (153)
18	EVA	ss3986147243	Apr 25, 2021 (155)
19	GNOMAD	ss4005742845	Apr 25, 2021 (155)
20	GNOMAD	ss4005742846	Apr 25, 2021 (155)
21	GNOMAD	ss4005742847	Apr 25, 2021 (155)
22	GNOMAD	ss4005742848	Apr 25, 2021 (155)
23	GNOMAD	ss4005742849	Apr 25, 2021 (155)
24	GNOMAD	ss4005742850	Apr 25, 2021 (155)
25	TOMMO_GENOMICS	ss5147011512	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5147011513	Apr 25, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5244699600	Oct 12, 2022 (156)
28	HUGCELL_USP	ss5445245399	Oct 12, 2022 (156)
29	HUGCELL_USP	ss5445245400	Oct 12, 2022 (156)
30	EVA	ss5623917308	Oct 12, 2022 (156)
31	SANFORD_IMAGENETICS	ss5626825795	Oct 12, 2022 (156)
32	TOMMO_GENOMICS	ss5674362200	Oct 12, 2022 (156)
33	TOMMO_GENOMICS	ss5674362201	Oct 12, 2022 (156)
34	YY_MCH	ss5801364185	Oct 12, 2022 (156)
35	EVA	ss5832828346	Oct 12, 2022 (156)
36	EVA	ss5832828347	Oct 12, 2022 (156)
37	EVA	ss5938629734	Oct 12, 2022 (156)
38	EVA	ss5979997834	Oct 12, 2022 (156)
39	The Danish reference pan genome	NC_000001.10 - 171252450	Apr 25, 2020 (154)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 30411892 (NC_000001.11:171283310::A 20483/59344) Row 30411893 (NC_000001.11:171283310::AA 236/59420) Row 30411894 (NC_000001.11:171283310::AAA 1/59428)...	-	Apr 25, 2021 (155)
46	Northern Sweden	NC_000001.10 - 171252450	Jul 12, 2019 (153)
47	8.3KJPN Submission ignored due to conflicting rows: Row 4980819 (NC_000001.10:171252449::A 123/16480) Row 4980820 (NC_000001.10:171252449:A: 7/16480)	-	Apr 25, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 4980819 (NC_000001.10:171252449::A 123/16480) Row 4980820 (NC_000001.10:171252449:A: 7/16480)	-	Apr 25, 2021 (155)
49	14KJPN Submission ignored due to conflicting rows: Row 8199304 (NC_000001.11:171283310::A 295/28080) Row 8199305 (NC_000001.11:171283310:A: 11/28080)	-	Oct 12, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 8199304 (NC_000001.11:171283310::A 295/28080) Row 8199305 (NC_000001.11:171283310:A: 11/28080)	-	Oct 12, 2022 (156)
51	ALFA	NC_000001.11 - 171283311	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).

Associated ID	History Updated (Build)
rs55953710	May 15, 2013 (138)
rs60924888	May 25, 2008 (130)
rs67171509	May 11, 2012 (137)
rs67171510	Feb 26, 2009 (130)
rs67171511	Feb 26, 2009 (130)
rs68074335	May 11, 2012 (137)
rs68074336	Feb 27, 2009 (130)
rs68074337	Feb 27, 2009 (130)
rs68074338	Feb 27, 2009 (130)
rs68074339	Feb 27, 2009 (130)
rs68074340	Feb 27, 2009 (130)
rs68074341	Feb 27, 2009 (130)
rs149740020	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4005742850	NC_000001.11:171283310:AA:	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAA	(self)
ss5147011513	NC_000001.10:171252449:A:	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAA	(self)
ss4005742849, ss5674362201	NC_000001.11:171283310:A:	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAA	(self)
ss326134375, ss551013040	NC_000001.9:169519073::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
180569, 875678, ss499033581, ss663131785, ss666115758, ss1574048480, ss1795263333, ss2985530708, ss3727590813, ss3986147243, ss5147011512, ss5623917308, ss5626825795, ss5832828346, ss5938629734, ss5979997834	NC_000001.10:171252449::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
ss3065334622, ss3645079607, ss3688013465, ss4005742845, ss5244699600, ss5445245399, ss5674362200, ss5801364185	NC_000001.11:171283310::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
ss77944025, ss287683097	NT_004487.19:22741091::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
ss32479826, ss82893350	NT_004487.19:22741100::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
ss193135588	NT_004487.20:28098723::A	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAA	(self)
ss5832828347	NC_000001.10:171252449::AA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAA
ss4005742846, ss5445245400	NC_000001.11:171283310::AA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAA	(self)
ss4005742847	NC_000001.11:171283310::AAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAA	(self)
ss4005742848	NC_000001.11:171283310::AAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAAAA	(self)
13166944585	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:171283310:AAAAAAAAA:A… NC_000001.11:171283310:AAAAAAAAA:AAAAAAAAAAAAAA	(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 rs28360426

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

rs28360426