SNP Links for Gene (Select 103352541) - SNP

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Items: 1 to 20 of 3335

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Select item 14910017481.

rs1491001748 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:139989213 (GRCh38)
6:140310350 (GRCh37)
Canonical SPDI:: NC_000006.12:139989212:G:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.139989213G>A, NC_000006.11:g.140310350G>A

Select item 14902834392.

rs1490283439 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:139983336 (GRCh38)
6:140304473 (GRCh37)
Canonical SPDI:: NC_000006.12:139983335:C:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0./0 (GnomAD)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139983336C>T, NC_000006.11:g.140304473C>T

Select item 14901851363.

rs1490185136 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 6:139989788 (GRCh38)
6:140310925 (GRCh37)
Canonical SPDI:: NC_000006.12:139989787:A:G,NC_000006.12:139989787:A:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
G=0.000546/1 (Korea1K)
HGVS:: NC_000006.12:g.139989788A>G, NC_000006.12:g.139989788A>T, NC_000006.11:g.140310925A>G, NC_000006.11:g.140310925A>T

Select item 14900095694.

rs1490009569 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:139983048 (GRCh38)
6:140304185 (GRCh37)
Canonical SPDI:: NC_000006.12:139983047:A:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.139983048A>G, NC_000006.11:g.140304185A>G, NG_078217.1:g.437A>G

Select item 14899535025.

rs1489953502 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139985571 (GRCh38)
6:140306708 (GRCh37)
Canonical SPDI:: NC_000006.12:139985570:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.139985571T>C, NC_000006.11:g.140306708T>C

Select item 14896376566.

rs1489637656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:139987303 (GRCh38)
6:140308440 (GRCh37)
Canonical SPDI:: NC_000006.12:139987302:C:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.139987303C>A, NC_000006.11:g.140308440C>A

Select item 14895598537.

rs1489559853 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:139979386 (GRCh38)
6:140300523 (GRCh37)
Canonical SPDI:: NC_000006.12:139979385:A:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139979386A>C, NC_000006.11:g.140300523A>C

Select item 14895355318.

rs1489535531 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:139979840 (GRCh38)
6:140300977 (GRCh37)
Canonical SPDI:: NC_000006.12:139979839:G:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.139979840G>T, NC_000006.11:g.140300977G>T

Select item 14892727069.

rs1489272706 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139987833 (GRCh38)
6:140308970 (GRCh37)
Canonical SPDI:: NC_000006.12:139987832:T:C
Gene:: LINC02941 (Varview), LOC103352541 (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_000006.12:g.139987833T>C, NC_000006.11:g.140308970T>C

Select item 148889172710.

rs1488891727 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139983353 (GRCh38)
6:140304490 (GRCh37)
Canonical SPDI:: NC_000006.12:139983352:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.139983353T>C, NC_000006.11:g.140304490T>C

Select item 148884315811.

rs1488843158 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:139987385 (GRCh38)
6:140308522 (GRCh37)
Canonical SPDI:: NC_000006.12:139987384:C:A
Gene:: LINC02941 (Varview), LOC103352541 (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_000006.12:g.139987385C>A, NC_000006.11:g.140308522C>A

Select item 148858193112.

rs1488581931 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:139991508 (GRCh38)
6:140312645 (GRCh37)
Canonical SPDI:: NC_000006.12:139991507:G:A,NC_000006.12:139991507:G:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.139991508G>A, NC_000006.12:g.139991508G>T, NC_000006.11:g.140312645G>A, NC_000006.11:g.140312645G>T

Select item 148853126613.

rs1488531266 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:139990390 (GRCh38)
6:140311527 (GRCh37)
Canonical SPDI:: NC_000006.12:139990389:C:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_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.139990390C>T, NC_000006.11:g.140311527C>T

Select item 148835880714.

rs1488358807 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:139992992 (GRCh38)
6:140314129 (GRCh37)
Canonical SPDI:: NC_000006.12:139992991:G:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.139992992G>A, NC_000006.11:g.140314129G>A

Select item 148830429815.

rs1488304298 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 6:139979465 (GRCh38)
6:140300602 (GRCh37)
Canonical SPDI:: NC_000006.12:139979464:G:
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.139979465del, NC_000006.11:g.140300602del

Select item 148827904516.

rs1488279045 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:139980772 (GRCh38)
6:140301909 (GRCh37)
Canonical SPDI:: NC_000006.12:139980771:G:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.00007/1 (ALFA)
HGVS:: NC_000006.12:g.139980772G>C, NC_000006.11:g.140301909G>C

Select item 148824693917.

rs1488246939 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:139984333 (GRCh38)
6:140305470 (GRCh37)
Canonical SPDI:: NC_000006.12:139984332:C:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.139984333C>G, NC_000006.11:g.140305470C>G

Select item 148763687718.

rs1487636877 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:139988238 (GRCh38)
6:140309375 (GRCh37)
Canonical SPDI:: NC_000006.12:139988237:G:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.139988238G>A, NC_000006.11:g.140309375G>A

Select item 148751776219.

rs1487517762 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 6:139990203 (GRCh38)
6:140311340 (GRCh37)
Canonical SPDI:: NC_000006.12:139990202:C:A,NC_000006.12:139990202:C:G,NC_000006.12:139990202:C:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000029/4 (GnomAD)
HGVS:: NC_000006.12:g.139990203C>A, NC_000006.12:g.139990203C>G, NC_000006.12:g.139990203C>T, NC_000006.11:g.140311340C>A, NC_000006.11:g.140311340C>G, NC_000006.11:g.140311340C>T

Select item 148693271020.

rs1486932710 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:139982551 (GRCh38)
6:140303688 (GRCh37)
Canonical SPDI:: NC_000006.12:139982550:T:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139982551T>G, NC_000006.11:g.140303688T>G

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