SNP Links for Gene (Select 100128682) - SNP

Links from Gene

Items: 1 to 20 of 3230

<< First< Prev

Page of 162

Next >Last >>

Select item 14913479421.

rs1491347942 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 19:35412097 (GRCh38)
19:35902999 (GRCh37)
Canonical SPDI:: NC_000019.10:35412095:TGT:T
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.35412097_35412098del, NC_000019.9:g.35902999_35903000del

Select item 14913028172.

rs1491302817 has merged into rs398040980 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:35413102 (GRCh38)
19:35904004 (GRCh37)
Canonical SPDI:: NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35413091:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.35413102_35413118del, NC_000019.10:g.35413103_35413118del, NC_000019.10:g.35413105_35413118del, NC_000019.10:g.35413106_35413118del, NC_000019.10:g.35413107_35413118del, NC_000019.10:g.35413108_35413118del, NC_000019.10:g.35413109_35413118del, NC_000019.10:g.35413110_35413118del, NC_000019.10:g.35413111_35413118del, NC_000019.10:g.35413112_35413118del, NC_000019.10:g.35413113_35413118del, NC_000019.10:g.35413114_35413118del, NC_000019.10:g.35413115_35413118del, NC_000019.10:g.35413116_35413118del, NC_000019.10:g.35413117_35413118del, NC_000019.10:g.35413118del, NC_000019.10:g.35413118dup, NC_000019.10:g.35413117_35413118dup, NC_000019.10:g.35413116_35413118dup, NC_000019.10:g.35413115_35413118dup, NC_000019.10:g.35413114_35413118dup, NC_000019.10:g.35413113_35413118dup, NC_000019.10:g.35413111_35413118dup, NC_000019.10:g.35413109_35413118dup, NC_000019.10:g.35413108_35413118dup, NC_000019.10:g.35413103_35413118dup, NC_000019.10:g.35413098_35413118dup, NC_000019.10:g.35413093_35413118dup, NC_000019.10:g.35413118_35413119insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.35904004_35904020del, NC_000019.9:g.35904005_35904020del, NC_000019.9:g.35904007_35904020del, NC_000019.9:g.35904008_35904020del, NC_000019.9:g.35904009_35904020del, NC_000019.9:g.35904010_35904020del, NC_000019.9:g.35904011_35904020del, NC_000019.9:g.35904012_35904020del, NC_000019.9:g.35904013_35904020del, NC_000019.9:g.35904014_35904020del, NC_000019.9:g.35904015_35904020del, NC_000019.9:g.35904016_35904020del, NC_000019.9:g.35904017_35904020del, NC_000019.9:g.35904018_35904020del, NC_000019.9:g.35904019_35904020del, NC_000019.9:g.35904020del, NC_000019.9:g.35904020dup, NC_000019.9:g.35904019_35904020dup, NC_000019.9:g.35904018_35904020dup, NC_000019.9:g.35904017_35904020dup, NC_000019.9:g.35904016_35904020dup, NC_000019.9:g.35904015_35904020dup, NC_000019.9:g.35904013_35904020dup, NC_000019.9:g.35904011_35904020dup, NC_000019.9:g.35904010_35904020dup, NC_000019.9:g.35904005_35904020dup, NC_000019.9:g.35904000_35904020dup, NC_000019.9:g.35903995_35904020dup, NC_000019.9:g.35904020_35904021insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14912034443.

rs1491203444 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 19:35408807 (GRCh38)
19:35899709 (GRCh37)
Canonical SPDI:: NC_000019.10:35408806:GT:
Gene:: LINC01531 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.017/85 (1000Genomes)
HGVS:: NC_000019.10:g.35408807_35408808del, NC_000019.9:g.35899709_35899710del, NR_040046.1:n.2298_2299del

Select item 14911984034.

rs1491198403 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 19:35413091 (GRCh38)
19:35903993 (GRCh37)
Canonical SPDI:: NC_000019.10:35413090:CT:
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000019.10:g.35413091_35413092del, NC_000019.9:g.35903993_35903994del

Select item 14910679455.

rs1491067945 has merged into rs11385018 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:35414380 (GRCh38)
19:35905282 (GRCh37)
Canonical SPDI:: NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35414366:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.2031/1017 (1000Genomes)
HGVS:: NC_000019.10:g.35414380_35414384del, NC_000019.10:g.35414381_35414384del, NC_000019.10:g.35414382_35414384del, NC_000019.10:g.35414383_35414384del, NC_000019.10:g.35414384del, NC_000019.10:g.35414384dup, NC_000019.10:g.35414383_35414384dup, NC_000019.10:g.35414382_35414384dup, NC_000019.10:g.35414380_35414384dup, NC_000019.10:g.35414379_35414384dup, NC_000019.10:g.35414373_35414384dup, NC_000019.10:g.35414368_35414384dup, NC_000019.10:g.35414384_35414385insAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.35905282_35905286del, NC_000019.9:g.35905283_35905286del, NC_000019.9:g.35905284_35905286del, NC_000019.9:g.35905285_35905286del, NC_000019.9:g.35905286del, NC_000019.9:g.35905286dup, NC_000019.9:g.35905285_35905286dup, NC_000019.9:g.35905284_35905286dup, NC_000019.9:g.35905282_35905286dup, NC_000019.9:g.35905281_35905286dup, NC_000019.9:g.35905275_35905286dup, NC_000019.9:g.35905270_35905286dup, NC_000019.9:g.35905286_35905287insAAAAAAAAAAAAAAAAAAAAA

Select item 14903160406.

rs1490316040 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35410769 (GRCh38)
19:35901671 (GRCh37)
Canonical SPDI:: NC_000019.10:35410768:A:G
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000069/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.35410769A>G, NC_000019.9:g.35901671A>G

Select item 14901271787.

rs1490127178 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TT [Show Flanks]
Chromosome:: 19:35403741 (GRCh38)
19:35894644 (GRCh37)
Canonical SPDI:: NC_000019.10:35403741:T:TTT
Gene:: LINC01531 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTT=0.0005/2 (ALFA)
TT=0.0002/1 (GnomAD)
HGVS:: NC_000019.10:g.35403742_35403743insTT, NC_000019.9:g.35894644_35894645insTT

Select item 14901026818.

rs1490102681 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 19:35404428 (GRCh38)
19:35895330 (GRCh37)
Canonical SPDI:: NC_000019.10:35404427:G:C,NC_000019.10:35404427:G:T
Gene:: LINC01531 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00626/104 (TOMMO)
T=0.13192/386 (KOREAN)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000019.10:g.35404428G>C, NC_000019.10:g.35404428G>T, NC_000019.9:g.35895330G>C, NC_000019.9:g.35895330G>T

Select item 14899771239.

rs1489977123 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:35404563 (GRCh38)
19:35895465 (GRCh37)
Canonical SPDI:: NC_000019.10:35404562:C:A
Gene:: LINC01531 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.35404563C>A, NC_000019.9:g.35895465C>A

Select item 148968620210.

rs1489686202 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:35407349 (GRCh38)
19:35898251 (GRCh37)
Canonical SPDI:: NC_000019.10:35407348:T:C
Gene:: LINC01531 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.0071/13 (Korea1K)
HGVS:: NC_000019.10:g.35407349T>C, NC_000019.9:g.35898251T>C, NR_040046.1:n.840T>C

Select item 148959766911.

rs1489597669 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:35411978 (GRCh38)
19:35902880 (GRCh37)
Canonical SPDI:: NC_000019.10:35411977:G:A
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000019.10:g.35411978G>A, NC_000019.9:g.35902880G>A

Select item 148930795612.

rs1489307956 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:35412094 (GRCh38)
19:35902996 (GRCh37)
Canonical SPDI:: NC_000019.10:35412093:T:G
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/2 (GnomAD)
G=0.000034/9 (TOPMED)
HGVS:: NC_000019.10:g.35412094T>G, NC_000019.9:g.35902996T>G

Select item 148897864013.

rs1488978640 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:35412946 (GRCh38)
19:35903848 (GRCh37)
Canonical SPDI:: NC_000019.10:35412945:T:A
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35412946T>A, NC_000019.9:g.35903848T>A

Select item 148885025414.

rs1488850254 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:35410283 (GRCh38)
19:35901185 (GRCh37)
Canonical SPDI:: NC_000019.10:35410282:C:G
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_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_000019.10:g.35410283C>G, NC_000019.9:g.35901185C>G

Select item 148856630915.

rs1488566309 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:35414847 (GRCh38)
19:35905749 (GRCh37)
Canonical SPDI:: NC_000019.10:35414846:G:T
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.35414847G>T, NC_000019.9:g.35905749G>T, NG_045111.1:g.403C>A

Select item 148842171816.

rs1488421718 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35408680 (GRCh38)
19:35899582 (GRCh37)
Canonical SPDI:: NC_000019.10:35408679:A:G
Gene:: LINC01531 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000009/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.35408680A>G, NC_000019.9:g.35899582A>G, NR_040046.1:n.2171A>G

Select item 148781237417.

rs1487812374 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35414191 (GRCh38)
19:35905093 (GRCh37)
Canonical SPDI:: NC_000019.10:35414190:A:G
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_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_000019.10:g.35414191A>G, NC_000019.9:g.35905093A>G

Select item 148763799518.

rs1487637995 has merged into rs970086872 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT,TTTTT,TTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:35412414 (GRCh38)
19:35903316 (GRCh37)
Canonical SPDI:: NC_000019.10:35412413:TTTTTTTT:TTTTTTT,NC_000019.10:35412413:TTTTTTTT:TTTTTTTTT,NC_000019.10:35412413:TTTTTTTT:TTTTTTTTTTTT,NC_000019.10:35412413:TTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:35412413:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35412413:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.00007/2 (TOMMO)
HGVS:: NC_000019.10:g.35412421del, NC_000019.10:g.35412421dup, NC_000019.10:g.35412418_35412421dup, NC_000019.10:g.35412414_35412421dup, NC_000019.10:g.35412421_35412422insTTTTTTTTTTTTTT, NC_000019.10:g.35412421_35412422insTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.35903323del, NC_000019.9:g.35903323dup, NC_000019.9:g.35903320_35903323dup, NC_000019.9:g.35903316_35903323dup, NC_000019.9:g.35903323_35903324insTTTTTTTTTTTTTT, NC_000019.9:g.35903323_35903324insTTTTTTTTTTTTTTTTTTTTT

Select item 148748207019.

rs1487482070 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:35414553 (GRCh38)
19:35905455 (GRCh37)
Canonical SPDI:: NC_000019.10:35414552:T:G
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35414553T>G, NC_000019.9:g.35905455T>G

Select item 148701950620.

rs1487019506 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:35413722 (GRCh38)
19:35904624 (GRCh37)
Canonical SPDI:: NC_000019.10:35413721:T:C
Gene:: LINC01531 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.35413722T>C, NC_000019.9:g.35904624T>C

<< First< Prev

Page of 162

Next >Last >>

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 3230

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity