SNP Links for Nucleotide (Select 338797703) - SNP

Links from Nucleotide

Items: 1 to 20 of 809

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Select item 14906896491.

rs1490689649 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:166349666 (GRCh38)
6:166763154 (GRCh37)
Canonical SPDI:: NC_000006.12:166349665:A:G
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166349666A>G, NC_000006.11:g.166763154A>G, NR_040022.1:n.2105A>G

Select item 14898730922.

rs1489873092 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:166350912 (GRCh38)
6:166764400 (GRCh37)
Canonical SPDI:: NC_000006.12:166350911:C:T
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166350912C>T, NC_000006.11:g.166764400C>T, NR_040022.1:n.3351C>T

Select item 14892337393.

rs1489233739 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:166349946 (GRCh38)
6:166763434 (GRCh37)
Canonical SPDI:: NC_000006.12:166349945:G:A
Gene:: LOC100289495 (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)
A=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.166349946G>A, NC_000006.11:g.166763434G>A, NR_040022.1:n.2385G>A

Select item 14891626054.

rs1489162605 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 6:166351149 (GRCh38)
6:166764637 (GRCh37)
Canonical SPDI:: NC_000006.12:166351148:G:
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.166351149del, NC_000006.11:g.166764637del, NR_040022.1:n.3588del

Select item 14889351865.

rs1488935186 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 6:166349469 (GRCh38)
6:166762957 (GRCh37)
Canonical SPDI:: NC_000006.12:166349468:A:C,NC_000006.12:166349468:A:G
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.166349469A>C, NC_000006.12:g.166349469A>G, NC_000006.11:g.166762957A>C, NC_000006.11:g.166762957A>G, NR_040022.1:n.1908A>C, NR_040022.1:n.1908A>G

Select item 14872016326.

rs1487201632 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:166350092 (GRCh38)
6:166763580 (GRCh37)
Canonical SPDI:: NC_000006.12:166350091:G:C
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_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_000006.12:g.166350092G>C, NC_000006.11:g.166763580G>C, NR_040022.1:n.2531G>C

Select item 14869460727.

rs1486946072 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:166349098 (GRCh38)
6:166762586 (GRCh37)
Canonical SPDI:: NC_000006.12:166349097:A:G
Gene:: LOC100289495 (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=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166349098A>G, NC_000006.11:g.166762586A>G, NR_040022.1:n.1537A>G

Select item 14869310538.

rs1486931053 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 6:166350633 (GRCh38)
6:166764121 (GRCh37)
Canonical SPDI:: NC_000006.12:166350632:C:
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166350633del, NC_000006.11:g.166764121del, NR_040022.1:n.3072del

Select item 14861254519.

rs1486125451 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:166348773 (GRCh38)
6:166762261 (GRCh37)
Canonical SPDI:: NC_000006.12:166348772:A:G
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.166348773A>G, NC_000006.11:g.166762261A>G, NR_040022.1:n.1212A>G

Select item 148402754410.

rs1484027544 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:166350722 (GRCh38)
6:166764211 (GRCh37)
Canonical SPDI:: NC_000006.12:166350722:T:TT
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.166350723dup, NC_000006.11:g.166764211dup, NR_040022.1:n.3162dup

Select item 148372455311.

rs1483724553 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:166342734 (GRCh38)
6:166756222 (GRCh37)
Canonical SPDI:: NC_000006.12:166342733:G:A
Gene:: SFT2D1 (Varview), LOC100289495 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.166342734G>A, NC_000006.11:g.166756222G>A, NR_040022.1:n.104G>A

Select item 148326885912.

rs1483268859 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:166343036 (GRCh38)
6:166756524 (GRCh37)
Canonical SPDI:: NC_000006.12:166343035:C:T
Gene:: SFT2D1 (Varview), LOC100289495 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166343036C>T, NC_000006.11:g.166756524C>T, NR_040022.1:n.406C>T

Select item 148136821313.

rs1481368213 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:166349100 (GRCh38)
6:166762588 (GRCh37)
Canonical SPDI:: NC_000006.12:166349099:T:A
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000006.12:g.166349100T>A, NC_000006.11:g.166762588T>A, NR_040022.1:n.1539T>A

Select item 147975808414.

rs1479758084 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:166350658 (GRCh38)
6:166764146 (GRCh37)
Canonical SPDI:: NC_000006.12:166350657:C:T
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.166350658C>T, NC_000006.11:g.166764146C>T, NR_040022.1:n.3097C>T

Select item 147962770415.

rs1479627704 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 6:166350105 (GRCh38)
6:166763593 (GRCh37)
Canonical SPDI:: NC_000006.12:166350104:A:C,NC_000006.12:166350104:A:T
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000034/9 (TOPMED)
T=0.000342/1 (KOREAN)
T=0.001092/2 (Korea1K)
HGVS:: NC_000006.12:g.166350105A>C, NC_000006.12:g.166350105A>T, NC_000006.11:g.166763593A>C, NC_000006.11:g.166763593A>T, NR_040022.1:n.2544A>C, NR_040022.1:n.2544A>T

Select item 147691209716.

rs1476912097 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:166349049 (GRCh38)
6:166762537 (GRCh37)
Canonical SPDI:: NC_000006.12:166349048:A:G
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.166349049A>G, NC_000006.11:g.166762537A>G, NR_040022.1:n.1488A>G

Select item 147610298717.

rs1476102987 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:166348219 (GRCh38)
6:166761707 (GRCh37)
Canonical SPDI:: NC_000006.12:166348218:G:A
Gene:: LOC100289495 (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_000006.12:g.166348219G>A, NC_000006.11:g.166761707G>A, NR_040022.1:n.658G>A

Select item 147544272518.

rs1475442725 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:166349109 (GRCh38)
6:166762597 (GRCh37)
Canonical SPDI:: NC_000006.12:166349108:T:C
Gene:: LOC100289495 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.166349109T>C, NC_000006.11:g.166762597T>C, NR_040022.1:n.1548T>C

Select item 147287654219.

rs1472876542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:166343092 (GRCh38)
6:166756580 (GRCh37)
Canonical SPDI:: NC_000006.12:166343091:G:A
Gene:: SFT2D1 (Varview), LOC100289495 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.166343092G>A, NC_000006.11:g.166756580G>A, NR_040022.1:n.462G>A

Select item 147254814920.

rs1472548149 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:166342721 (GRCh38)
6:166756209 (GRCh37)
Canonical SPDI:: NC_000006.12:166342720:C:A,NC_000006.12:166342720:C:T
Gene:: SFT2D1 (Varview), LOC100289495 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.166342721C>A, NC_000006.12:g.166342721C>T, NC_000006.11:g.166756209C>A, NC_000006.11:g.166756209C>T, NR_040022.1:n.91C>A, NR_040022.1:n.91C>T

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