SNP Links for Gene (Select 440594) - SNP

Links from Gene

Items: 1 to 20 of 1529

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Select item 14908908451.

rs1490890845 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:95473617 (GRCh38)
1:95939173 (GRCh37)
Canonical SPDI:: NC_000001.11:95473616:A:G
Gene:: LINC01761 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.95473617A>G, NC_000001.10:g.95939173A>G

Select item 14908599882.

rs1490859988 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:95474650 (GRCh38)
1:95940206 (GRCh37)
Canonical SPDI:: NC_000001.11:95474649:T:C
Gene:: LINC01761 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000156/1 (1000Genomes)
HGVS:: NC_000001.11:g.95474650T>C, NC_000001.10:g.95940206T>C

Select item 14907608503.

rs1490760850 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:95478302 (GRCh38)
1:95943858 (GRCh37)
Canonical SPDI:: NC_000001.11:95478301:T:C
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95478302T>C, NC_000001.10:g.95943858T>C, NR_033966.1:n.1701T>C

Select item 14900716964.

rs1490071696 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:95474126 (GRCh38)
1:95939682 (GRCh37)
Canonical SPDI:: NC_000001.11:95474125:A:C
Gene:: LINC01761 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.95474126A>C, NC_000001.10:g.95939682A>C

Select item 14900411825.

rs1490041182 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:95475132 (GRCh38)
1:95940688 (GRCh37)
Canonical SPDI:: NC_000001.11:95475131:A:G
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.95475132A>G, NC_000001.10:g.95940688A>G, NR_033966.1:n.396A>G

Select item 14900195046.

rs1490019504 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:95476714 (GRCh38)
1:95942270 (GRCh37)
Canonical SPDI:: NC_000001.11:95476713:C:T
Gene:: LINC01761 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.95476714C>T, NC_000001.10:g.95942270C>T

Select item 14891504557.

rs1489150455 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:95473409 (GRCh38)
1:95938965 (GRCh37)
Canonical SPDI:: NC_000001.11:95473408:T:G
Gene:: LINC01761 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95473409T>G, NC_000001.10:g.95938965T>G

Select item 14884334218.

rs1488433421 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:95476813 (GRCh38)
1:95942369 (GRCh37)
Canonical SPDI:: NC_000001.11:95476812:A:G
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.95476813A>G, NC_000001.10:g.95942369A>G, NR_033966.1:n.570A>G

Select item 14883160949.

rs1488316094 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:95476074 (GRCh38)
1:95941630 (GRCh37)
Canonical SPDI:: NC_000001.11:95476073:A:G
Gene:: LINC01761 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.95476074A>G, NC_000001.10:g.95941630A>G

Select item 148828417310.

rs1488284173 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:95477714 (GRCh38)
1:95943270 (GRCh37)
Canonical SPDI:: NC_000001.11:95477713:G:A
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95477714G>A, NC_000001.10:g.95943270G>A, NR_033966.1:n.1113G>A

Select item 148798473111.

rs1487984731 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:95476585 (GRCh38)
1:95942141 (GRCh37)
Canonical SPDI:: NC_000001.11:95476584:G:A
Gene:: LINC01761 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95476585G>A, NC_000001.10:g.95942141G>A

Select item 148664947612.

rs1486649476 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:95478224 (GRCh38)
1:95943780 (GRCh37)
Canonical SPDI:: NC_000001.11:95478223:C:T
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.95478224C>T, NC_000001.10:g.95943780C>T, NR_033966.1:n.1623C>T

Select item 148647913213.

rs1486479132 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:95479061 (GRCh38)
1:95944617 (GRCh37)
Canonical SPDI:: NC_000001.11:95479060:C:A
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.95479061C>A, NC_000001.10:g.95944617C>A, NR_033966.1:n.2460C>A

Select item 148635363014.

rs1486353630 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:95477121 (GRCh38)
1:95942677 (GRCh37)
Canonical SPDI:: NC_000001.11:95477120:T:G
Gene:: LINC01761 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95477121T>G, NC_000001.10:g.95942677T>G

Select item 148632135115.

rs1486321351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:95478732 (GRCh38)
1:95944288 (GRCh37)
Canonical SPDI:: NC_000001.11:95478731:C:G,NC_000001.11:95478731:C:T
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.95478732C>G, NC_000001.11:g.95478732C>T, NC_000001.10:g.95944288C>G, NC_000001.10:g.95944288C>T, NR_033966.1:n.2131C>G, NR_033966.1:n.2131C>T

Select item 148617990116.

rs1486179901 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:95479759 (GRCh38)
1:95945315 (GRCh37)
Canonical SPDI:: NC_000001.11:95479758:T:A,NC_000001.11:95479758:T:C
Gene:: LINC01761 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.95479759T>A, NC_000001.11:g.95479759T>C, NC_000001.10:g.95945315T>A, NC_000001.10:g.95945315T>C

Select item 148572045617.

rs1485720456 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:95478757 (GRCh38)
1:95944313 (GRCh37)
Canonical SPDI:: NC_000001.11:95478756:A:G
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.95478757A>G, NC_000001.10:g.95944313A>G, NR_033966.1:n.2156A>G

Select item 148559697118.

rs1485596971 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:95475433 (GRCh38)
1:95940989 (GRCh37)
Canonical SPDI:: NC_000001.11:95475432:T:C
Gene:: LINC01761 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.95475433T>C, NC_000001.10:g.95940989T>C

Select item 148480637119.

rs1484806371 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:95474089 (GRCh38)
1:95939645 (GRCh37)
Canonical SPDI:: NC_000001.11:95474088:C:A
Gene:: LINC01761 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0.00007/1 (ALFA)
HGVS:: NC_000001.11:g.95474089C>A, NC_000001.10:g.95939645C>A

Select item 148360447620.

rs1483604476 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:95477556 (GRCh38)
1:95943112 (GRCh37)
Canonical SPDI:: NC_000001.11:95477555:C:T
Gene:: LINC01761 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.95477556C>T, NC_000001.10:g.95943112C>T, NR_033966.1:n.955C>T

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