Name: rs1491491022
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.

rs1491491022

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:154198664 (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: insCAA / insCACAA / ins(CA)₃A / in…
insCAA / insCACAA / ins(CA)₃A / ins(CA)₄A
Variation Type: Indel Insertion and Deletion
Frequency: insCACAA=0.00007 (2/28258, 14KJPN)
insCACAA=0.00006 (1/16760, 8.3KJPN)
insCAA=0.00000 (0/11860, ALFA) (+ 3 more)
insCACAA=0.00000 (0/11860, ALFA)
ins(CA)₃A=0.00000 (0/11860, ALFA)
ins(CA)₄A=0.00000 (0/11860, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OPRM1 : Intron Variant
IPCEF1 : 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	11860	A=1.00000	ACAA=0.00000, ACACAA=0.00000, ACACACAA=0.00000, ACACACACAA=0.00000	1.0	N/A
European	Sub	7618	A=1.0000	ACAA=0.0000, ACACAA=0.0000, ACACACAA=0.0000, ACACACACAA=0.0000	1.0	N/A
African	Sub	2816	A=1.0000	ACAA=0.0000, ACACAA=0.0000, ACACACAA=0.0000, ACACACACAA=0.0000	1.0	N/A
African Others	Sub	108	A=1.000	ACAA=0.000, ACACAA=0.000, ACACACAA=0.000, ACACACACAA=0.000	1.0	N/A
African American	Sub	2708	A=1.0000	ACAA=0.0000, ACACAA=0.0000, ACACACAA=0.0000, ACACACACAA=0.0000	1.0	N/A
Asian	Sub	108	A=1.000	ACAA=0.000, ACACAA=0.000, ACACACAA=0.000, ACACACACAA=0.000	1.0	N/A
East Asian	Sub	84	A=1.00	ACAA=0.00, ACACAA=0.00, ACACACAA=0.00, ACACACACAA=0.00	1.0	N/A
Other Asian	Sub	24	A=1.00	ACAA=0.00, ACACAA=0.00, ACACACAA=0.00, ACACACACAA=0.00	1.0	N/A
Latin American 1	Sub	146	A=1.000	ACAA=0.000, ACACAA=0.000, ACACACAA=0.000, ACACACACAA=0.000	1.0	N/A
Latin American 2	Sub	610	A=1.000	ACAA=0.000, ACACAA=0.000, ACACACAA=0.000, ACACACACAA=0.000	1.0	N/A
South Asian	Sub	94	A=1.00	ACAA=0.00, ACACAA=0.00, ACACACAA=0.00, ACACACACAA=0.00	1.0	N/A
Other	Sub	468	A=1.000	ACAA=0.000, ACACAA=0.000, ACACACAA=0.000, ACACACACAA=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
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	insCACAA=0.00007
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	insCACAA=0.00006
Allele Frequency Aggregator	Total	Global	11860	A=1.00000	insCAA=0.00000, insCACAA=0.00000, ins(CA)₃A=0.00000, ins(CA)₄A=0.00000
Allele Frequency Aggregator	European	Sub	7618	A=1.0000	insCAA=0.0000, insCACAA=0.0000, ins(CA)₃A=0.0000, ins(CA)₄A=0.0000
Allele Frequency Aggregator	African	Sub	2816	A=1.0000	insCAA=0.0000, insCACAA=0.0000, ins(CA)₃A=0.0000, ins(CA)₄A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	A=1.000	insCAA=0.000, insCACAA=0.000, ins(CA)₃A=0.000, ins(CA)₄A=0.000
Allele Frequency Aggregator	Other	Sub	468	A=1.000	insCAA=0.000, insCACAA=0.000, ins(CA)₃A=0.000, ins(CA)₄A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	A=1.000	insCAA=0.000, insCACAA=0.000, ins(CA)₃A=0.000, ins(CA)₄A=0.000
Allele Frequency Aggregator	Asian	Sub	108	A=1.000	insCAA=0.000, insCACAA=0.000, ins(CA)₃A=0.000, ins(CA)₄A=0.000
Allele Frequency Aggregator	South Asian	Sub	94	A=1.00	insCAA=0.00, insCACAA=0.00, ins(CA)₃A=0.00, ins(CA)₄A=0.00

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 6	NC_000006.12:g.154198664_154198665insCAA
GRCh38.p14 chr 6	NC_000006.12:g.154198664AC[2]AA[1]
GRCh38.p14 chr 6	NC_000006.12:g.154198664AC[3]AA[1]
GRCh38.p14 chr 6	NC_000006.12:g.154198664AC[4]AA[1]
GRCh37.p13 chr 6	NC_000006.11:g.154519798_154519799insCAA
GRCh37.p13 chr 6	NC_000006.11:g.154519798AC[2]AA[1]
GRCh37.p13 chr 6	NC_000006.11:g.154519798AC[3]AA[1]
GRCh37.p13 chr 6	NC_000006.11:g.154519798AC[4]AA[1]
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.193164_193165insCAA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.193164AC[2]AA[1]
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.193164AC[3]AA[1]
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.193164AC[4]AA[1]

Gene: OPRM1, opioid receptor mu 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1165-480… NM_001008503.3:c.1165-48029_1165-48028insCAA	N/A	Intron Variant
OPRM1 transcript variant MOR-1	NM_000914.5:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A	NM_001008504.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1X	NM_001008505.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1i	NM_001145279.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G1	NM_001145280.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G2	NM_001145281.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B1	NM_001145282.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B2	NM_001145283.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B3	NM_001145284.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B4	NM_001145285.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B5	NM_001145286.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K1	NM_001145287.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1S	NM_001285522.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A2	NM_001285523.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1CA	NM_001285524.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K2	NM_001285526.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1W	NM_001285527.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-3	NM_001285528.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y3	NR_104348.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y2	NR_104349.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Z	NR_104350.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y	NR_104351.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X2	XM_011535851.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X3	XM_011535853.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X5	XM_011535856.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X7	XM_011535862.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X1	XM_017010903.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X4	XM_017010904.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X8	XM_017010907.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X6	XM_047418837.1:c.	N/A	Genic Downstream Transcript Variant

Gene: IPCEF1, interaction protein for cytohesin exchange factors 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IPCEF1 transcript variant 1	NM_001130699.2:c.910+1004… NM_001130699.2:c.910+1004_910+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 2	NM_001130700.2:c.910+1004… NM_001130700.2:c.910+1004_910+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 4	NM_001394799.1:c.910+1004… NM_001394799.1:c.910+1004_910+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 5	NM_001394800.1:c.910+1004… NM_001394800.1:c.910+1004_910+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 6	NM_001394801.1:c.910+1004… NM_001394801.1:c.910+1004_910+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 7	NM_001394802.1:c.907+1004… NM_001394802.1:c.907+1004_907+1005insTTG	N/A	Intron Variant
IPCEF1 transcript variant 3	NM_015553.3:c.907+1004_90… NM_015553.3:c.907+1004_907+1005insTTG	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=	insCAA	insCACAA	ins(CA)₃A	ins(CA)₄A
GRCh38.p14 chr 6	NC_000006.12:g.154198664=	NC_000006.12:g.154198664_154198665insCAA	NC_000006.12:g.154198664AC[2]AA[1]	NC_000006.12:g.154198664AC[3]AA[1]	NC_000006.12:g.154198664AC[4]AA[1]
GRCh37.p13 chr 6	NC_000006.11:g.154519798=	NC_000006.11:g.154519798_154519799insCAA	NC_000006.11:g.154519798AC[2]AA[1]	NC_000006.11:g.154519798AC[3]AA[1]	NC_000006.11:g.154519798AC[4]AA[1]
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.193164=	NG_021208.2:g.193164_193165insCAA	NG_021208.2:g.193164AC[2]AA[1]	NG_021208.2:g.193164AC[3]AA[1]	NG_021208.2:g.193164AC[4]AA[1]
OPRM1 transcript variant MOR-1O	NM_001008503.1:c.1165-48029=	NM_001008503.1:c.1165-48029_1165-48028insCAA	NM_001008503.1:c.1165-48029_1165-48028insCACAA	NM_001008503.1:c.1165-48029_1165-48028insCACACAA	NM_001008503.1:c.1165-48029_1165-48028insCACACACAA
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1165-48029=	NM_001008503.3:c.1165-48029_1165-48028insCAA	NM_001008503.3:c.1165-48029_1165-48028insCACAA	NM_001008503.3:c.1165-48029_1165-48028insCACACAA	NM_001008503.3:c.1165-48029_1165-48028insCACACACAA
IPCEF1 transcript variant 1	NM_001130699.1:c.910+1004=	NM_001130699.1:c.910+1004_910+1005insTTG	NM_001130699.1:c.910+1004_910+1005insTTGTG	NM_001130699.1:c.910+1004_910+1005insTTGTGTG	NM_001130699.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 1	NM_001130699.2:c.910+1004=	NM_001130699.2:c.910+1004_910+1005insTTG	NM_001130699.2:c.910+1004_910+1005insTTGTG	NM_001130699.2:c.910+1004_910+1005insTTGTGTG	NM_001130699.2:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 2	NM_001130700.1:c.910+1004=	NM_001130700.1:c.910+1004_910+1005insTTG	NM_001130700.1:c.910+1004_910+1005insTTGTG	NM_001130700.1:c.910+1004_910+1005insTTGTGTG	NM_001130700.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 2	NM_001130700.2:c.910+1004=	NM_001130700.2:c.910+1004_910+1005insTTG	NM_001130700.2:c.910+1004_910+1005insTTGTG	NM_001130700.2:c.910+1004_910+1005insTTGTGTG	NM_001130700.2:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 4	NM_001394799.1:c.910+1004=	NM_001394799.1:c.910+1004_910+1005insTTG	NM_001394799.1:c.910+1004_910+1005insTTGTG	NM_001394799.1:c.910+1004_910+1005insTTGTGTG	NM_001394799.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 5	NM_001394800.1:c.910+1004=	NM_001394800.1:c.910+1004_910+1005insTTG	NM_001394800.1:c.910+1004_910+1005insTTGTG	NM_001394800.1:c.910+1004_910+1005insTTGTGTG	NM_001394800.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 6	NM_001394801.1:c.910+1004=	NM_001394801.1:c.910+1004_910+1005insTTG	NM_001394801.1:c.910+1004_910+1005insTTGTG	NM_001394801.1:c.910+1004_910+1005insTTGTGTG	NM_001394801.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant 7	NM_001394802.1:c.907+1004=	NM_001394802.1:c.907+1004_907+1005insTTG	NM_001394802.1:c.907+1004_907+1005insTTGTG	NM_001394802.1:c.907+1004_907+1005insTTGTGTG	NM_001394802.1:c.907+1004_907+1005insTTGTGTGTG
IPCEF1 transcript variant 3	NM_015553.2:c.907+1004=	NM_015553.2:c.907+1004_907+1005insTTG	NM_015553.2:c.907+1004_907+1005insTTGTG	NM_015553.2:c.907+1004_907+1005insTTGTGTG	NM_015553.2:c.907+1004_907+1005insTTGTGTGTG
IPCEF1 transcript variant 3	NM_015553.3:c.907+1004=	NM_015553.3:c.907+1004_907+1005insTTG	NM_015553.3:c.907+1004_907+1005insTTGTG	NM_015553.3:c.907+1004_907+1005insTTGTGTG	NM_015553.3:c.907+1004_907+1005insTTGTGTGTG
IPCEF1 transcript variant X1	XM_005266919.1:c.910+1004=	XM_005266919.1:c.910+1004_910+1005insTTG	XM_005266919.1:c.910+1004_910+1005insTTGTG	XM_005266919.1:c.910+1004_910+1005insTTGTGTG	XM_005266919.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant X2	XM_005266920.1:c.910+1004=	XM_005266920.1:c.910+1004_910+1005insTTG	XM_005266920.1:c.910+1004_910+1005insTTGTG	XM_005266920.1:c.910+1004_910+1005insTTGTGTG	XM_005266920.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant X3	XM_005266921.1:c.910+1004=	XM_005266921.1:c.910+1004_910+1005insTTG	XM_005266921.1:c.910+1004_910+1005insTTGTG	XM_005266921.1:c.910+1004_910+1005insTTGTGTG	XM_005266921.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant X4	XM_005266922.1:c.910+1004=	XM_005266922.1:c.910+1004_910+1005insTTG	XM_005266922.1:c.910+1004_910+1005insTTGTG	XM_005266922.1:c.910+1004_910+1005insTTGTGTG	XM_005266922.1:c.910+1004_910+1005insTTGTGTGTG
IPCEF1 transcript variant X5	XM_005266923.1:c.907+1004=	XM_005266923.1:c.907+1004_907+1005insTTG	XM_005266923.1:c.907+1004_907+1005insTTGTG	XM_005266923.1:c.907+1004_907+1005insTTGTGTG	XM_005266923.1:c.907+1004_907+1005insTTGTGTGTG

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#.

5 SubSNP, 6 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4154406202	Apr 26, 2021 (155)
2	GNOMAD	ss4154406203	Apr 26, 2021 (155)
3	GNOMAD	ss4154406204	Apr 26, 2021 (155)
4	TOMMO_GENOMICS	ss5180699535	Apr 26, 2021 (155)
5	TOMMO_GENOMICS	ss5719801150	Oct 14, 2022 (156)
6	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246115739 (NC_000006.12:154198663::ACA 19/138372) Row 246115740 (NC_000006.12:154198663::ACACA 1/138374) Row 246115741 (NC_000006.12:154198663::ACACACA 1/138374)	-	Apr 26, 2021 (155)
7	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246115739 (NC_000006.12:154198663::ACA 19/138372) Row 246115740 (NC_000006.12:154198663::ACACA 1/138374) Row 246115741 (NC_000006.12:154198663::ACACACA 1/138374)	-	Apr 26, 2021 (155)
8	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246115739 (NC_000006.12:154198663::ACA 19/138372) Row 246115740 (NC_000006.12:154198663::ACACA 1/138374) Row 246115741 (NC_000006.12:154198663::ACACACA 1/138374)	-	Apr 26, 2021 (155)
9	8.3KJPN	NC_000006.11 - 154519798	Apr 26, 2021 (155)
10	14KJPN	NC_000006.12 - 154198664	Oct 14, 2022 (156)
11	ALFA	NC_000006.12 - 154198664	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4154406202	NC_000006.12:154198663::ACA	NC_000006.12:154198663:A:ACAA	(self)
5364618744	NC_000006.12:154198663:A:ACAA	NC_000006.12:154198663:A:ACAA	(self)
38668842, ss5180699535	NC_000006.11:154519797::ACACA	NC_000006.12:154198663:A:ACACAA	(self)
53638254, ss4154406203, ss5719801150	NC_000006.12:154198663::ACACA	NC_000006.12:154198663:A:ACACAA	(self)
5364618744	NC_000006.12:154198663:A:ACACAA	NC_000006.12:154198663:A:ACACAA	(self)
ss4154406204	NC_000006.12:154198663::ACACACA	NC_000006.12:154198663:A:ACACACAA	(self)
5364618744	NC_000006.12:154198663:A:ACACACAA	NC_000006.12:154198663:A:ACACACAA	(self)
5364618744	NC_000006.12:154198663:A:ACACACACAA	NC_000006.12:154198663:A:ACACACACAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3516383088	NC_000006.12:154198663::ACACACACA	NC_000006.12:154198663:A:ACACACACAA

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

No publications for rs1491491022

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

rs1491491022