Name: rs374305646
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.

rs374305646

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:46890279-46890296 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₇ / ins(A)₂₀ / ins(A)₁₄C(A)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.1757 (880/5008, 1000G)
delAAA=0.000 (0/892, ALFA)
delAA=0.000 (0/892, ALFA) (+ 5 more)
delA=0.000 (0/892, ALFA)
dupA=0.000 (0/892, ALFA)
dupAA=0.000 (0/892, ALFA)
dupAAA=0.000 (0/892, ALFA)
dup(A)₄=0.000 (0/892, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP4Z2P : 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	892	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	184	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	638	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	612	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	10	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	10	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	28	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.1757
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.1082
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.0923
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.3290
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.175
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.205
Allele Frequency Aggregator	Total	Global	892	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	African	Sub	638	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	European	Sub	184	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	28	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(A)₁₈=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	10	(A)₁₈=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Asian	Sub	8	(A)₁₈=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.46890294_46890296del
GRCh38.p14 chr 1	NC_000001.11:g.46890295_46890296del
GRCh38.p14 chr 1	NC_000001.11:g.46890296del
GRCh38.p14 chr 1	NC_000001.11:g.46890296dup
GRCh38.p14 chr 1	NC_000001.11:g.46890295_46890296dup
GRCh38.p14 chr 1	NC_000001.11:g.46890294_46890296dup
GRCh38.p14 chr 1	NC_000001.11:g.46890293_46890296dup
GRCh38.p14 chr 1	NC_000001.11:g.46890290_46890296dup
GRCh38.p14 chr 1	NC_000001.11:g.46890296_46890297insAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.46890279_46890296A[32]CAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 1	NC_000001.10:g.47355966_47355968del
GRCh37.p13 chr 1	NC_000001.10:g.47355967_47355968del
GRCh37.p13 chr 1	NC_000001.10:g.47355968del
GRCh37.p13 chr 1	NC_000001.10:g.47355968dup
GRCh37.p13 chr 1	NC_000001.10:g.47355967_47355968dup
GRCh37.p13 chr 1	NC_000001.10:g.47355966_47355968dup
GRCh37.p13 chr 1	NC_000001.10:g.47355965_47355968dup
GRCh37.p13 chr 1	NC_000001.10:g.47355962_47355968dup
GRCh37.p13 chr 1	NC_000001.10:g.47355968_47355969insAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.47355951_47355968A[32]CAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Gene: CYP4Z2P, cytochrome P450 family 4 subfamily Z member 2, pseudogene (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP4Z2P transcript	NR_002788.2: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)₁₈=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₇	ins(A)₂₀	ins(A)₁₄C(A)₂₇
GRCh38.p14 chr 1	NC_000001.11:g.46890279_46890296=	NC_000001.11:g.46890294_46890296del	NC_000001.11:g.46890295_46890296del	NC_000001.11:g.46890296del	NC_000001.11:g.46890296dup	NC_000001.11:g.46890295_46890296dup	NC_000001.11:g.46890294_46890296dup	NC_000001.11:g.46890293_46890296dup	NC_000001.11:g.46890290_46890296dup	NC_000001.11:g.46890296_46890297insAAAAAAAAAAAAAAAAAAAA	NC_000001.11:g.46890279_46890296A[32]CAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 1	NC_000001.10:g.47355951_47355968=	NC_000001.10:g.47355966_47355968del	NC_000001.10:g.47355967_47355968del	NC_000001.10:g.47355968del	NC_000001.10:g.47355968dup	NC_000001.10:g.47355967_47355968dup	NC_000001.10:g.47355966_47355968dup	NC_000001.10:g.47355965_47355968dup	NC_000001.10:g.47355962_47355968dup	NC_000001.10:g.47355968_47355969insAAAAAAAAAAAAAAAAAAAA	NC_000001.10:g.47355951_47355968A[32]CAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

43 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41342403	Oct 11, 2018 (152)
2	HUMANGENOME_JCVI	ss95228324	Oct 11, 2018 (152)
3	PJP	ss294577503	Oct 11, 2018 (152)
4	BILGI_BIOE	ss666090480	Apr 25, 2013 (138)
5	1000GENOMES	ss1367698912	Aug 21, 2014 (142)
6	SWEGEN	ss2986730703	Nov 08, 2017 (151)
7	SWEGEN	ss2986730704	Nov 08, 2017 (151)
8	MCHAISSO	ss3063586541	Nov 08, 2017 (151)
9	URBANLAB	ss3646653645	Oct 11, 2018 (152)
10	EVA_DECODE	ss3686669275	Jul 12, 2019 (153)
11	EVA_DECODE	ss3686669276	Jul 12, 2019 (153)
12	EVA_DECODE	ss3686669277	Jul 12, 2019 (153)
13	EVA_DECODE	ss3686669278	Jul 12, 2019 (153)
14	EVA_DECODE	ss3686669279	Jul 12, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3799149970	Jul 12, 2019 (153)
16	EVA	ss3826148138	Apr 25, 2020 (154)
17	GNOMAD	ss3992709359	Apr 25, 2021 (155)
18	GNOMAD	ss3992709360	Apr 25, 2021 (155)
19	GNOMAD	ss3992709361	Apr 25, 2021 (155)
20	GNOMAD	ss3992709362	Apr 25, 2021 (155)
21	GNOMAD	ss3992709363	Apr 25, 2021 (155)
22	GNOMAD	ss3992709364	Apr 25, 2021 (155)
23	GNOMAD	ss3992709365	Apr 25, 2021 (155)
24	GNOMAD	ss3992709366	Apr 25, 2021 (155)
25	TOMMO_GENOMICS	ss5143701690	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5143701691	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5143701692	Apr 25, 2021 (155)
28	TOMMO_GENOMICS	ss5143701693	Apr 25, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5242084581	Oct 17, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5242084582	Oct 17, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5242084583	Oct 17, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5242084584	Oct 17, 2022 (156)
33	HUGCELL_USP	ss5443167700	Oct 17, 2022 (156)
34	HUGCELL_USP	ss5443167701	Oct 17, 2022 (156)
35	HUGCELL_USP	ss5443167702	Oct 17, 2022 (156)
36	HUGCELL_USP	ss5443167703	Oct 17, 2022 (156)
37	TOMMO_GENOMICS	ss5668398129	Oct 17, 2022 (156)
38	TOMMO_GENOMICS	ss5668398130	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5668398131	Oct 17, 2022 (156)
40	TOMMO_GENOMICS	ss5668398132	Oct 17, 2022 (156)
41	EVA	ss5831888904	Oct 17, 2022 (156)
42	EVA	ss5831888905	Oct 17, 2022 (156)
43	EVA	ss5848885368	Oct 17, 2022 (156)
44	1000Genomes	NC_000001.10 - 47355951	Oct 11, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 9813364 (NC_000001.11:46890278::A 81887/107922) Row 9813365 (NC_000001.11:46890278::AA 713/108014) Row 9813366 (NC_000001.11:46890278::AAA 167/108080)...	-	Apr 25, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 1670997 (NC_000001.10:47355950::A 10757/16626) Row 1670998 (NC_000001.10:47355950:A: 9/16626) Row 1670999 (NC_000001.10:47355950::AA 48/16626)...	-	Apr 25, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 1670997 (NC_000001.10:47355950::A 10757/16626) Row 1670998 (NC_000001.10:47355950:A: 9/16626) Row 1670999 (NC_000001.10:47355950::AA 48/16626)...	-	Apr 25, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 1670997 (NC_000001.10:47355950::A 10757/16626) Row 1670998 (NC_000001.10:47355950:A: 9/16626) Row 1670999 (NC_000001.10:47355950::AA 48/16626)...	-	Apr 25, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 1670997 (NC_000001.10:47355950::A 10757/16626) Row 1670998 (NC_000001.10:47355950:A: 9/16626) Row 1670999 (NC_000001.10:47355950::AA 48/16626)...	-	Apr 25, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 2235233 (NC_000001.11:46890278::A 19041/28162) Row 2235234 (NC_000001.11:46890278::AA 83/28162) Row 2235235 (NC_000001.11:46890278:A: 15/28162)...	-	Oct 17, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 2235233 (NC_000001.11:46890278::A 19041/28162) Row 2235234 (NC_000001.11:46890278::AA 83/28162) Row 2235235 (NC_000001.11:46890278:A: 15/28162)...	-	Oct 17, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 2235233 (NC_000001.11:46890278::A 19041/28162) Row 2235234 (NC_000001.11:46890278::AA 83/28162) Row 2235235 (NC_000001.11:46890278:A: 15/28162)...	-	Oct 17, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 2235233 (NC_000001.11:46890278::A 19041/28162) Row 2235234 (NC_000001.11:46890278::AA 83/28162) Row 2235235 (NC_000001.11:46890278:A: 15/28162)...	-	Oct 17, 2022 (156)
61	ALFA	NC_000001.11 - 46890279	Apr 25, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3992709366	NC_000001.11:46890278:AAA:	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3686669279, ss3992709365, ss5443167703, ss5668398132	NC_000001.11:46890278:AA:	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5143701691	NC_000001.10:47355950:A:	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3992709364, ss5242084584, ss5443167700, ss5668398131	NC_000001.11:46890278:A:	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3686669278	NC_000001.11:46890279:A:	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss294577503	NC_000001.9:47128555::A	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
1389427, ss666090480, ss1367698912, ss2986730703, ss3826148138, ss5143701690, ss5831888904	NC_000001.10:47355950::A	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3063586541, ss3646653645, ss3799149970, ss3992709359, ss5242084581, ss5443167701, ss5668398129, ss5848885368	NC_000001.11:46890278::A	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3686669277	NC_000001.11:46890280::A	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss41342403, ss95228324	NT_032977.9:17327886::A	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss2986730704, ss5143701692, ss5831888905	NC_000001.10:47355950::AA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3992709360, ss5242084582, ss5443167702, ss5668398130	NC_000001.11:46890278::AA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3686669276	NC_000001.11:46890280::AA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3992709361	NC_000001.11:46890278::AAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3992709362, ss5242084583	NC_000001.11:46890278::AAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
2630181735	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686669275	NC_000001.11:46890280::AAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5143701693	NC_000001.10:47355950::AAAAAAAAAAA… NC_000001.10:47355950::AAAAAAAAAAAAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3992709363	NC_000001.11:46890278::AAAAAAAAAAA… NC_000001.11:46890278::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAA	NC_000001.11:46890278:AAAAAAAAAAAA… NC_000001.11:46890278:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs374305646

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

rs374305646