SNP Links for Nucleotide (Select 1190332602) - SNP

Links from Nucleotide

Items: 1 to 20 of 371

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Select item 14906466971.

rs1490646697 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:155395125 (GRCh38)
7:155187820 (GRCh37)
Canonical SPDI:: NC_000007.14:155395124:A:C
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.155395125A>C, NC_000007.13:g.155187820A>C, NR_147174.1:n.320A>C

Select item 14903580412.

rs1490358041 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:155382090 (GRCh38)
7:155174785 (GRCh37)
Canonical SPDI:: NC_000007.14:155382089:G:A
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.0003/1 (KOREAN)
HGVS:: NC_000007.14:g.155382090G>A, NC_000007.13:g.155174785G>A, NR_147174.1:n.15G>A

Select item 14895365623.

rs1489536562 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:155395123 (GRCh38)
7:155187818 (GRCh37)
Canonical SPDI:: NC_000007.14:155395122:G:A
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000014/2 (GnomAD_exomes)
HGVS:: NC_000007.14:g.155395123G>A, NC_000007.13:g.155187818G>A, NR_147174.1:n.318G>A

Select item 14873169834.

rs1487316983 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:155395131 (GRCh38)
7:155187826 (GRCh37)
Canonical SPDI:: NC_000007.14:155395130:G:C
Gene:: LINC03010 (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_000007.14:g.155395131G>C, NC_000007.13:g.155187826G>C, NR_147174.1:n.326G>C

Select item 14867703355.

rs1486770335 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 7:155382117 (GRCh38)
7:155174812 (GRCh37)
Canonical SPDI:: NC_000007.14:155382116:A:C,NC_000007.14:155382116:A:T
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
T=0.000559/1 (Korea1K)
HGVS:: NC_000007.14:g.155382117A>C, NC_000007.14:g.155382117A>T, NC_000007.13:g.155174812A>C, NC_000007.13:g.155174812A>T, NR_147174.1:n.42A>C, NR_147174.1:n.42A>T

Select item 14824085896.

rs1482408589 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:155401477 (GRCh38)
7:155194172 (GRCh37)
Canonical SPDI:: NC_000007.14:155401476:T:C
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.155401477T>C, NC_000007.13:g.155194172T>C, NR_147174.1:n.991T>C

Select item 14817029617.

rs1481702961 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:155395048 (GRCh38)
7:155187743 (GRCh37)
Canonical SPDI:: NC_000007.14:155395047:G:A,NC_000007.14:155395047:G:C
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.155395048G>A, NC_000007.14:g.155395048G>C, NC_000007.13:g.155187743G>A, NC_000007.13:g.155187743G>C, NR_147174.1:n.243G>A, NR_147174.1:n.243G>C

Select item 14780392638.

rs1478039263 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:155401627 (GRCh38)
7:155194322 (GRCh37)
Canonical SPDI:: NC_000007.14:155401626:A:C
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.155401627A>C, NC_000007.13:g.155194322A>C, NR_147174.1:n.1141A>C

Select item 14764044189.

rs1476404418 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:155401071 (GRCh38)
7:155193766 (GRCh37)
Canonical SPDI:: NC_000007.14:155401070:T:G
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.155401071T>G, NC_000007.13:g.155193766T>G, NR_147174.1:n.585T>G

Select item 147454599310.

rs1474545993 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:155401406 (GRCh38)
7:155194101 (GRCh37)
Canonical SPDI:: NC_000007.14:155401405:A:G,NC_000007.14:155401405:A:T
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000007.14:g.155401406A>G, NC_000007.14:g.155401406A>T, NC_000007.13:g.155194101A>G, NC_000007.13:g.155194101A>T, NR_147174.1:n.920A>G, NR_147174.1:n.920A>T

Select item 147199479911.

rs1471994799 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:155401551 (GRCh38)
7:155194246 (GRCh37)
Canonical SPDI:: NC_000007.14:155401550:C:T
Gene:: LINC03010 (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_000007.14:g.155401551C>T, NC_000007.13:g.155194246C>T, NR_147174.1:n.1065C>T

Select item 147111721912.

rs1471117219 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:155401615 (GRCh38)
7:155194310 (GRCh37)
Canonical SPDI:: NC_000007.14:155401614:C:G
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.155401615C>G, NC_000007.13:g.155194310C>G, NR_147174.1:n.1129C>G

Select item 147110615113.

rs1471106151 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:155401188 (GRCh38)
7:155193883 (GRCh37)
Canonical SPDI:: NC_000007.14:155401187:T:A
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.155401188T>A, NC_000007.13:g.155193883T>A, NR_147174.1:n.702T>A

Select item 146836601814.

rs1468366018 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:155382176 (GRCh38)
7:155174871 (GRCh37)
Canonical SPDI:: NC_000007.14:155382175:G:C
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.155382176G>C, NC_000007.13:g.155174871G>C, NR_147174.1:n.101G>C

Select item 146603813915.

rs1466038139 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:155401594 (GRCh38)
7:155194289 (GRCh37)
Canonical SPDI:: NC_000007.14:155401593:C:A
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.155401594C>A, NC_000007.13:g.155194289C>A, NR_147174.1:n.1108C>A

Select item 146475119016.

rs1464751190 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:155401221 (GRCh38)
7:155193916 (GRCh37)
Canonical SPDI:: NC_000007.14:155401220:G:T
Gene:: LINC03010 (Varview)
Functional Consequence:: 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_000007.14:g.155401221G>T, NC_000007.13:g.155193916G>T, NR_147174.1:n.735G>T

Select item 146461161817.

rs1464611618 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:155401297 (GRCh38)
7:155193992 (GRCh37)
Canonical SPDI:: NC_000007.14:155401296:G:A
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (KOREAN)
A=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.155401297G>A, NC_000007.13:g.155193992G>A, NR_147174.1:n.811G>A

Select item 146355169818.

rs1463551698 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:155401533 (GRCh38)
7:155194228 (GRCh37)
Canonical SPDI:: NC_000007.14:155401532:C:G,NC_000007.14:155401532:C:T
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.155401533C>G, NC_000007.14:g.155401533C>T, NC_000007.13:g.155194228C>G, NC_000007.13:g.155194228C>T, NR_147174.1:n.1047C>G, NR_147174.1:n.1047C>T

Select item 146245403919.

rs1462454039 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:155382308 (GRCh38)
7:155175003 (GRCh37)
Canonical SPDI:: NC_000007.14:155382307:A:G
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.155382308A>G, NC_000007.13:g.155175003A>G, NR_147174.1:n.233A>G

Select item 145763699820.

rs1457636998 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 7:155395205 (GRCh38)
7:155187900 (GRCh37)
Canonical SPDI:: NC_000007.14:155395204:A:C,NC_000007.14:155395204:A:T
Gene:: LINC03010 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000111/1 (ALFA)
T=0.000007/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.155395205A>C, NC_000007.14:g.155395205A>T, NC_000007.13:g.155187900A>C, NC_000007.13:g.155187900A>T, NR_147174.1:n.400A>C, NR_147174.1:n.400A>T

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