SNP Links for Nucleotide (Select 213021173) - SNP

Links from Nucleotide

Items: 1 to 20 of 351

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Select item 14855260881.

rs1485526088 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:46855950 (GRCh38)
2:47083089 (GRCh37)
Canonical SPDI:: NC_000002.12:46855949:G:A
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000002.12:g.46855950G>A, NC_000002.11:g.47083089G>A, NR_024452.1:n.249G>A

Select item 14829017352.

rs1482901735 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:46858964 (GRCh38)
2:47086103 (GRCh37)
Canonical SPDI:: NC_000002.12:46858963:A:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.46858964A>T, NC_000002.11:g.47086103A>T, NR_024452.1:n.1168A>T

Select item 14814652883.

rs1481465288 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:46855957 (GRCh38)
2:47083096 (GRCh37)
Canonical SPDI:: NC_000002.12:46855956:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.46855957C>T, NC_000002.11:g.47083096C>T, NR_024452.1:n.256C>T

Select item 14805295544.

rs1480529554 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:46858124 (GRCh38)
2:47085263 (GRCh37)
Canonical SPDI:: NC_000002.12:46858123:A:G
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD_exomes)
G=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.46858124A>G, NC_000002.11:g.47085263A>G, NR_024452.1:n.328A>G

Select item 14791736775.

rs1479173677 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:46858360 (GRCh38)
2:47085499 (GRCh37)
Canonical SPDI:: NC_000002.12:46858359:T:C
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.46858360T>C, NC_000002.11:g.47085499T>C, NR_024452.1:n.564T>C

Select item 14770991106.

rs1477099110 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:46855985 (GRCh38)
2:47083124 (GRCh37)
Canonical SPDI:: NC_000002.12:46855984:T:C
Gene:: LINC01119 (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_000002.12:g.46855985T>C, NC_000002.11:g.47083124T>C, NR_024452.1:n.284T>C

Select item 14757646737.

rs1475764673 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:46827954 (GRCh38)
2:47055093 (GRCh37)
Canonical SPDI:: NC_000002.12:46827953:G:A
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000002.12:g.46827954G>A, NC_000002.11:g.47055093G>A, NR_024452.1:n.91G>A

Select item 14754893258.

rs1475489325 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:46858638 (GRCh38)
2:47085777 (GRCh37)
Canonical SPDI:: NC_000002.12:46858637:A:G
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.46858638A>G, NC_000002.11:g.47085777A>G, NR_024452.1:n.842A>G

Select item 14754166079.

rs1475416607 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:46858500 (GRCh38)
2:47085639 (GRCh37)
Canonical SPDI:: NC_000002.12:46858499:T:G
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.46858500T>G, NC_000002.11:g.47085639T>G, NR_024452.1:n.704T>G

Select item 147316744610.

rs1473167446 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:46855969 (GRCh38)
2:47083108 (GRCh37)
Canonical SPDI:: NC_000002.12:46855968:G:A
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.46855969G>A, NC_000002.11:g.47083108G>A, NR_024452.1:n.268G>A

Select item 147286414011.

rs1472864140 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:46858239 (GRCh38)
2:47085378 (GRCh37)
Canonical SPDI:: NC_000002.12:46858238:A:G
Gene:: LINC01119 (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=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.46858239A>G, NC_000002.11:g.47085378A>G, NR_024452.1:n.443A>G

Select item 146662724712.

rs1466627247 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:46858835 (GRCh38)
2:47085974 (GRCh37)
Canonical SPDI:: NC_000002.12:46858834:G:A
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000002.12:g.46858835G>A, NC_000002.11:g.47085974G>A, NR_024452.1:n.1039G>A

Select item 146425628513.

rs1464256285 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 2:46828021 (GRCh38)
2:47055160 (GRCh37)
Canonical SPDI:: NC_000002.12:46828020:C:G,NC_000002.12:46828020:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.46828021C>G, NC_000002.12:g.46828021C>T, NC_000002.11:g.47055160C>G, NC_000002.11:g.47055160C>T, NR_024452.1:n.158C>G, NR_024452.1:n.158C>T

Select item 146400682014.

rs1464006820 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:46858277 (GRCh38)
2:47085416 (GRCh37)
Canonical SPDI:: NC_000002.12:46858276:G:A
Gene:: LINC01119 (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_000002.12:g.46858277G>A, NC_000002.11:g.47085416G>A, NR_024452.1:n.481G>A

Select item 145819789215.

rs1458197892 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:46858339 (GRCh38)
2:47085478 (GRCh37)
Canonical SPDI:: NC_000002.12:46858338:T:C
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.46858339T>C, NC_000002.11:g.47085478T>C, NR_024452.1:n.543T>C

Select item 145783500216.

rs1457835002 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:46828041 (GRCh38)
2:47055180 (GRCh37)
Canonical SPDI:: NC_000002.12:46828040:C:G
Gene:: LINC01119 (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=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.46828041C>G, NC_000002.11:g.47055180C>G, NR_024452.1:n.178C>G

Select item 145736968917.

rs1457369689 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:46858194 (GRCh38)
2:47085333 (GRCh37)
Canonical SPDI:: NC_000002.12:46858193:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000013/2 (GnomAD_exomes)
T=0.000021/3 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000002.12:g.46858194C>T, NC_000002.11:g.47085333C>T, NR_024452.1:n.398C>T

Select item 145133581618.

rs1451335816 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:46858883 (GRCh38)
2:47086022 (GRCh37)
Canonical SPDI:: NC_000002.12:46858882:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.46858883C>T, NC_000002.11:g.47086022C>T, NR_024452.1:n.1087C>T

Select item 145006169819.

rs1450061698 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:46858170 (GRCh38)
2:47085309 (GRCh37)
Canonical SPDI:: NC_000002.12:46858169:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.46858170C>T, NC_000002.11:g.47085309C>T, NR_024452.1:n.374C>T

Select item 144744321220.

rs1447443212 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:46858807 (GRCh38)
2:47085946 (GRCh37)
Canonical SPDI:: NC_000002.12:46858806:C:T
Gene:: LINC01119 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.46858807C>T, NC_000002.11:g.47085946C>T, NR_024452.1:n.1011C>T

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