SNP Links for Gene (Select 693207) - SNP

Links from Gene

Items: 1 to 20 of 681

<< First< Prev

Page of 35

Next >Last >>

Select item 14903807321.

rs1490380732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:90229447 (GRCh38)
13:90881701 (GRCh37)
Canonical SPDI:: NC_000013.11:90229446:G:C
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000013.11:g.90229447G>C, NC_000013.10:g.90881701G>C

Select item 14900567902.

rs1490056790 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:90231002 (GRCh38)
13:90883256 (GRCh37)
Canonical SPDI:: NC_000013.11:90231001:A:C
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_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_000013.11:g.90231002A>C, NC_000013.10:g.90883256A>C, NG_009656.1:g.772A>C

Select item 14898655253.

rs1489865525 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:90230262 (GRCh38)
13:90882516 (GRCh37)
Canonical SPDI:: NC_000013.11:90230261:G:A
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00054/10 (ALFA)
A=0.000034/9 (TOPMED)
A=0.000086/12 (GnomAD)
A=0.002009/9 (Estonian)
HGVS:: NC_000013.11:g.90230262G>A, NC_000013.10:g.90882516G>A, NG_009656.1:g.32G>A

Select item 14890004994.

rs1489000499 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:90229776 (GRCh38)
13:90882030 (GRCh37)
Canonical SPDI:: NC_000013.11:90229775:C:T
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000038/10 (TOPMED)
HGVS:: NC_000013.11:g.90229776C>T, NC_000013.10:g.90882030C>T

Select item 14887460355.

rs1488746035 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:90231107 (GRCh38)
13:90883361 (GRCh37)
Canonical SPDI:: NC_000013.11:90231106:C:A
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000013.11:g.90231107C>A, NC_000013.10:g.90883361C>A, NG_009656.1:g.877C>A

Select item 14865692286.

rs1486569228 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:90229491 (GRCh38)
13:90881745 (GRCh37)
Canonical SPDI:: NC_000013.11:90229490:G:A
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000013.11:g.90229491G>A, NC_000013.10:g.90881745G>A

Select item 14846452277.

rs1484645227 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 13:90230786 (GRCh38)
13:90883040 (GRCh37)
Canonical SPDI:: NC_000013.11:90230785:C:G,NC_000013.11:90230785:C:T
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000358/6 (TOMMO)
HGVS:: NC_000013.11:g.90230786C>G, NC_000013.11:g.90230786C>T, NC_000013.10:g.90883040C>G, NC_000013.10:g.90883040C>T, NG_009656.1:g.556C>G, NG_009656.1:g.556C>T

Select item 14830701088.

rs1483070108 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:90229197 (GRCh38)
13:90881451 (GRCh37)
Canonical SPDI:: NC_000013.11:90229196:A:G
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.90229197A>G, NC_000013.10:g.90881451A>G

Select item 14817039349.

rs1481703934 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 13:90229694 (GRCh38)
13:90881948 (GRCh37)
Canonical SPDI:: NC_000013.11:90229693:T:C,NC_000013.11:90229693:T:G
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000023/6 (TOPMED)
G=0.000283/5 (TOMMO)
HGVS:: NC_000013.11:g.90229694T>C, NC_000013.11:g.90229694T>G, NC_000013.10:g.90881948T>C, NC_000013.10:g.90881948T>G

Select item 148053123210.

rs1480531232 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:90229477 (GRCh38)
13:90881731 (GRCh37)
Canonical SPDI:: NC_000013.11:90229476:G:C
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000013.11:g.90229477G>C, NC_000013.10:g.90881731G>C

Select item 147987097111.

rs1479870971 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:90230303 (GRCh38)
13:90882557 (GRCh37)
Canonical SPDI:: NC_000013.11:90230302:A:G
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.90230303A>G, NC_000013.10:g.90882557A>G, NG_009656.1:g.73A>G

Select item 147791061512.

rs1477910615 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:90229339 (GRCh38)
13:90881593 (GRCh37)
Canonical SPDI:: NC_000013.11:90229338:G:T
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000013.11:g.90229339G>T, NC_000013.10:g.90881593G>T

Select item 147766970413.

rs1477669704 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:90231203 (GRCh38)
13:90883457 (GRCh37)
Canonical SPDI:: NC_000013.11:90231202:G:T
Gene:: MIR622 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000013.11:g.90231203G>T, NC_000013.10:g.90883457G>T, NG_009656.1:g.973G>T, NR_030754.1:n.22G>T

Select item 147697963414.

rs1476979634 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 13:90231276 (GRCh38)
13:90883530 (GRCh37)
Canonical SPDI:: NC_000013.11:90231275:C:A,NC_000013.11:90231275:C:T
Gene:: MIR622 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.90231276C>A, NC_000013.11:g.90231276C>T, NC_000013.10:g.90883530C>A, NC_000013.10:g.90883530C>T, NG_009656.1:g.1046C>A, NG_009656.1:g.1046C>T, NR_030754.1:n.95C>A, NR_030754.1:n.95C>T

Select item 147617208515.

rs1476172085 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:90230598 (GRCh38)
13:90882852 (GRCh37)
Canonical SPDI:: NC_000013.11:90230597:G:A
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000013.11:g.90230598G>A, NC_000013.10:g.90882852G>A, NG_009656.1:g.368G>A

Select item 147596999016.

rs1475969990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:90231755 (GRCh38)
13:90884009 (GRCh37)
Canonical SPDI:: NC_000013.11:90231754:A:G
Gene:: MIR622 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_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_000013.11:g.90231755A>G, NC_000013.10:g.90884009A>G, NG_009656.1:g.1525A>G

Select item 147563674917.

rs1475636749 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:90231436 (GRCh38)
13:90883690 (GRCh37)
Canonical SPDI:: NC_000013.11:90231435:T:A
Gene:: MIR622 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.90231436T>A, NC_000013.10:g.90883690T>A, NG_009656.1:g.1206T>A

Select item 147510523918.

rs1475105239 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:90229986 (GRCh38)
13:90882240 (GRCh37)
Canonical SPDI:: NC_000013.11:90229985:C:T
Gene:: MIR622 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_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_000013.11:g.90229986C>T, NC_000013.10:g.90882240C>T

Select item 147119124119.

rs1471191241 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:90231501 (GRCh38)
13:90883755 (GRCh37)
Canonical SPDI:: NC_000013.11:90231500:G:A
Gene:: MIR622 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.90231501G>A, NC_000013.10:g.90883755G>A, NG_009656.1:g.1271G>A

Select item 147085054620.

rs1470850546 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:90229969 (GRCh38)
13:90882223 (GRCh37)
Canonical SPDI:: NC_000013.11:90229968:G:T
Gene:: MIR622 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000013.11:g.90229969G>T, NC_000013.10:g.90882223G>T

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 681

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity