SNP Links for Gene (Select 105369473) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 5047

<< First< Prev

Page of 253

Next >Last >>

Select item 14908796131.

rs1490879613 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:106122837 (GRCh38)
11:105993564 (GRCh37)
Canonical SPDI:: NC_000011.10:106122836:C:A
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
A=0.000177/3 (TOMMO)
A=0.000342/1 (KOREAN)
HGVS:: NC_000011.10:g.106122837C>A, NC_000011.9:g.105993564C>A

Select item 14908464462.

rs1490846446 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 11:106133139 (GRCh38)
11:106003866 (GRCh37)
Canonical SPDI:: NC_000011.10:106133138:AA:A
Gene:: LINC02719 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
-=0.000093/13 (GnomAD)
-=0.000204/54 (TOPMED)
HGVS:: NC_000011.10:g.106133140del, NC_000011.9:g.106003867del

Select item 14907201663.

rs1490720166 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:106116728 (GRCh38)
11:105987455 (GRCh37)
Canonical SPDI:: NC_000011.10:106116727:C:A
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.00007/1 (ALFA)
HGVS:: NC_000011.10:g.106116728C>A, NC_000011.9:g.105987455C>A

Select item 14905110374.

rs1490511037 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:106118630 (GRCh38)
11:105989357 (GRCh37)
Canonical SPDI:: NC_000011.10:106118629:A:T
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00738/33 (Estonian)
T=0.0373/109 (KOREAN)
HGVS:: NC_000011.10:g.106118630A>T, NC_000011.9:g.105989357A>T

Select item 14904682375.

rs1490468237 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:106130638 (GRCh38)
11:106001365 (GRCh37)
Canonical SPDI:: NC_000011.10:106130637:C:T
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.106130638C>T, NC_000011.9:g.106001365C>T

Select item 14900213986.

rs1490021398 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:106112454 (GRCh38)
11:105983181 (GRCh37)
Canonical SPDI:: NC_000011.10:106112453:A:G
Gene:: LINC02719 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.106112454A>G, NC_000011.9:g.105983181A>G

Select item 14898754937.

rs1489875493 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:106121020 (GRCh38)
11:105991747 (GRCh37)
Canonical SPDI:: NC_000011.10:106121019:G:A
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.106121020G>A, NC_000011.9:g.105991747G>A

Select item 14896956408.

rs1489695640 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:106114731 (GRCh38)
11:105985458 (GRCh37)
Canonical SPDI:: NC_000011.10:106114730:A:C
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_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_000011.10:g.106114731A>C, NC_000011.9:g.105985458A>C

Select item 14896065389.

rs1489606538 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:106120914 (GRCh38)
11:105991641 (GRCh37)
Canonical SPDI:: NC_000011.10:106120913:A:C,NC_000011.10:106120913:A:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.106120914A>C, NC_000011.10:g.106120914A>G, NC_000011.9:g.105991641A>C, NC_000011.9:g.105991641A>G

Select item 148941194710.

rs1489411947 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:106114437 (GRCh38)
11:105985164 (GRCh37)
Canonical SPDI:: NC_000011.10:106114436:G:A
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.106114437G>A, NC_000011.9:g.105985164G>A

Select item 148937305411.

rs1489373054 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAGA>- [Show Flanks]
Chromosome:: 11:106113635 (GRCh38)
11:105984362 (GRCh37)
Canonical SPDI:: NC_000011.10:106113633:AAAGA:A
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.106113635_106113638del, NC_000011.9:g.105984362_105984365del

Select item 148933647812.

rs1489336478 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:106131499 (GRCh38)
11:106002226 (GRCh37)
Canonical SPDI:: NC_000011.10:106131498:A:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.106131499A>G, NC_000011.9:g.106002226A>G

Select item 148931119113.

rs1489311191 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:106118344 (GRCh38)
11:105989071 (GRCh37)
Canonical SPDI:: NC_000011.10:106118343:C:A,NC_000011.10:106118343:C:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.106118344C>A, NC_000011.10:g.106118344C>G, NC_000011.9:g.105989071C>A, NC_000011.9:g.105989071C>G

Select item 148919446014.

rs1489194460 [Homo sapiens]

Variant type:: DEL
Alleles:: AAACT>- [Show Flanks]
Chromosome:: 11:106113573 (GRCh38)
11:105984300 (GRCh37)
Canonical SPDI:: NC_000011.10:106113572:AAACT:
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000011.10:g.106113573_106113577del, NC_000011.9:g.105984300_105984304del

Select item 148915226215.

rs1489152262 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:106125368 (GRCh38)
11:105996095 (GRCh37)
Canonical SPDI:: NC_000011.10:106125367:A:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00006/16 (TOPMED)
HGVS:: NC_000011.10:g.106125368A>G, NC_000011.9:g.105996095A>G

Select item 148904377616.

rs1489043776 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:106120160 (GRCh38)
11:105990887 (GRCh37)
Canonical SPDI:: NC_000011.10:106120159:C:T
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.106120160C>T, NC_000011.9:g.105990887C>T

Select item 148879172317.

rs1488791723 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:106124187 (GRCh38)
11:105994914 (GRCh37)
Canonical SPDI:: NC_000011.10:106124186:C:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000468/3 (1000Genomes)
HGVS:: NC_000011.10:g.106124187C>G, NC_000011.9:g.105994914C>G

Select item 148861374918.

rs1488613749 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 11:106125789 (GRCh38)
11:105996516 (GRCh37)
Canonical SPDI:: NC_000011.10:106125788:T:
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000054/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.106125789del, NC_000011.9:g.105996516del

Select item 148856867019.

rs1488568670 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:106128132 (GRCh38)
11:105998859 (GRCh37)
Canonical SPDI:: NC_000011.10:106128131:A:G
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_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_000011.10:g.106128132A>G, NC_000011.9:g.105998859A>G

Select item 148821982720.

rs1488219827 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:106125038 (GRCh38)
11:105995765 (GRCh37)
Canonical SPDI:: NC_000011.10:106125037:G:A,NC_000011.10:106125037:G:T
Gene:: LINC02719 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.106125038G>A, NC_000011.10:g.106125038G>T, NC_000011.9:g.105995765G>A, NC_000011.9:g.105995765G>T