SNP Links for Nucleotide (Select 747172696) - SNP

Select item 12302748551.

rs1230274855 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:97416255 (GRCh38)
2:97957444 (GRCh37)
Canonical SPDI:: NC_000002.12:97416254:T:C
Gene:: LINC02969 (Varview), LOC107985920 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
HGVS:: NC_000002.12:g.97416255T>C, NC_000002.11:g.97957444A>G, NW_025791765.1:g.391049T>C, NR_130704.1:n.616A>G

Select item 10397989282.

rs1039798928 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:97284920 (GRCh38)
2:97950657 (GRCh37)
Canonical SPDI:: NC_000002.12:97284919:A:G
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000002.12:g.97284920A>G, NC_000002.11:g.97950657A>G, NW_025791765.1:g.259618A>G, NR_040097.2:n.2323A>G, NR_103733.1:n.378A>G, NR_103732.1:n.167A>G, NR_040097.1:n.2323A>G

Select item 10299185823.

rs1029918582 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 10230509934.

rs1023050993 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 10170861885.

rs1017086188 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:97284148 (GRCh38)
2:97949885 (GRCh37)
Canonical SPDI:: NC_000002.12:97284147:G:C
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000002.12:g.97284148G>C, NC_000002.11:g.97949885G>C, NW_025791765.1:g.258846G>C, NR_040097.2:n.1643G>C, NR_103733.1:n.214G>C, NR_040097.1:n.1643G>C

Select item 10170565706.

rs1017056570 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:97284739 (GRCh38)
2:97950476 (GRCh37)
Canonical SPDI:: NC_000002.12:97284738:G:A
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000002.12:g.97284739G>A, NC_000002.11:g.97950476G>A, NW_025791765.1:g.259437G>A, NR_040097.2:n.2234G>A, NR_103733.1:n.289G>A, NR_103732.1:n.78G>A, NR_040097.1:n.2234G>A

Select item 10134781737.

rs1013478173 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 10106557818.

rs1010655781 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 10043728159.

rs1004372815 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:97284782 (GRCh38)
2:97950519 (GRCh37)
Canonical SPDI:: NC_000002.12:97284781:G:T
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.00006/1 (TOMMO)
HGVS:: NC_000002.12:g.97284782G>T, NC_000002.11:g.97950519G>T, NW_025791765.1:g.259480G>T, NR_040097.2:n.2277G>T, NR_103733.1:n.332G>T, NR_103732.1:n.121G>T, NR_040097.1:n.2277G>T

Select item 99823924010.

rs998239240 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:97284905 (GRCh38)
2:97950642 (GRCh37)
Canonical SPDI:: NC_000002.12:97284904:C:A
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000002.12:g.97284905C>A, NC_000002.11:g.97950642C>A, NW_025791765.1:g.259603C>A, NR_040097.2:n.2308C>A, NR_103733.1:n.363C>A, NR_103732.1:n.152C>A, NR_040097.1:n.2308C>A

Select item 96279288411.

rs962792884 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 89951295212.

rs899512952 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>T
Chromosome:: no mapping
Canonical SPDI:

Select item 57058653213.

rs570586532 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:97284884 (GRCh38)
2:97950621 (GRCh37)
Canonical SPDI:: NC_000002.12:97284883:A:C
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.0002/1 (1000Genomes)
HGVS:: NC_000002.12:g.97284884A>C, NC_000002.11:g.97950621A>C, NW_025791765.1:g.259582A>C, NR_040097.2:n.2287A>C, NR_103733.1:n.342A>C, NR_103732.1:n.131A>C, NR_040097.1:n.2287A>C

Select item 56307163114.

rs563071631 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:97284163 (GRCh38)
2:97949900 (GRCh37)
Canonical SPDI:: NC_000002.12:97284162:A:C
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.0002/1 (1000Genomes)
HGVS:: NC_000002.12:g.97284163A>C, NC_000002.11:g.97949900A>C, NW_025791765.1:g.258861A>C, NR_040097.2:n.1658A>C, NR_103733.1:n.229A>C, NR_040097.1:n.1658A>C

Select item 53197428515.

rs531974285 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:97284158 (GRCh38)
2:97949895 (GRCh37)
Canonical SPDI:: NC_000002.12:97284157:A:C,NC_000002.12:97284157:A:G
Gene:: LOC100506076 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0004/2 (ALFA)
G=0.0004/2 (1000Genomes)
HGVS:: NC_000002.12:g.97284158A>C, NC_000002.12:g.97284158A>G, NC_000002.11:g.97949895A>C, NC_000002.11:g.97949895A>G, NW_025791765.1:g.258856A>C, NW_025791765.1:g.258856A>G, NR_040097.2:n.1653A>C, NR_040097.2:n.1653A>G, NR_103733.1:n.224A>C, NR_103733.1:n.224A>G, NR_040097.1:n.1653A>C, NR_040097.1:n.1653A>G

Select item 11278515216.

rs112785152 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:97284047 (GRCh38)
2:97949784 (GRCh37)
Canonical SPDI:: NC_000002.12:97284046:A:C
Gene:: LOC100506076 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000002.12:g.97284047A>C, NC_000002.11:g.97949784A>C, NW_025791765.1:g.258745A>C, NR_040097.2:n.1542A>C, NR_103733.1:n.113A>C, NR_040097.1:n.1542A>C

Select item 11152108117.

rs111521081 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 2:97284036 (GRCh38)
2:97949773 (GRCh37)
Canonical SPDI:: NC_000002.12:97284035:T:A,NC_000002.12:97284035:T:G
Gene:: LOC100506076 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000002.12:g.97284036T>A, NC_000002.12:g.97284036T>G, NC_000002.11:g.97949773T>A, NC_000002.11:g.97949773T>G, NW_025791765.1:g.258734T>A, NW_025791765.1:g.258734T>G, NR_040097.2:n.1531T>A, NR_040097.2:n.1531T>G, NR_103733.1:n.102T>A, NR_103733.1:n.102T>G, NR_040097.1:n.1531T>A, NR_040097.1:n.1531T>G

Select item 245891818.

rs2458918 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 2:97284080 (GRCh38)
2:97949817 (GRCh37)
Canonical SPDI:: NC_000002.12:97284079:A:G,NC_000002.12:97284079:A:T
Gene:: LOC100506076 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.0007/3 (ALFA)
HGVS:: NC_000002.12:g.97284080A>G, NC_000002.12:g.97284080A>T, NC_000002.11:g.97949817A>G, NC_000002.11:g.97949817A>T, NW_025791765.1:g.258778A>G, NW_025791765.1:g.258778A>T, NR_040097.2:n.1575A>G, NR_040097.2:n.1575A>T, NR_103733.1:n.146A>G, NR_103733.1:n.146A>T, NR_040097.1:n.1575A>G, NR_040097.1:n.1575A>T

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Links from Nucleotide

Items: 18

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