SNP Links for Gene (Select 131) - SNP

Links from Gene

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Select item 14908315861.

rs1490831586 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:99423374 (GRCh38)
4:100344531 (GRCh37)
Canonical SPDI:: NC_000004.12:99423373:G:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000004.12:g.99423374G>A, NC_000004.11:g.100344531G>A

Select item 14907985652.

rs1490798565 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:99419189 (GRCh38)
4:100340346 (GRCh37)
Canonical SPDI:: NC_000004.12:99419188:G:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.99419189G>A, NC_000004.11:g.100340346G>A

Select item 14906645623.

rs1490664562 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:99423061 (GRCh38)
4:100344218 (GRCh37)
Canonical SPDI:: NC_000004.12:99423060:T:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/1 (GnomAD)
HGVS:: NC_000004.12:g.99423061T>C, NC_000004.11:g.100344218T>C

Select item 14905232434.

rs1490523243 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:99416988 (GRCh38)
4:100338145 (GRCh37)
Canonical SPDI:: NC_000004.12:99416987:G:A,NC_000004.12:99416987:G:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.99416988G>A, NC_000004.12:g.99416988G>C, NC_000004.11:g.100338145G>A, NC_000004.11:g.100338145G>C

Select item 14904801305.

rs1490480130 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:99415595 (GRCh38)
4:100336752 (GRCh37)
Canonical SPDI:: NC_000004.12:99415594:A:G
Gene:: ADH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.99415595A>G, NC_000004.11:g.100336752A>G, NM_000673.7:c.983T>C, NM_000673.6:c.1019T>C, NM_000673.5:c.1019T>C, NM_000673.4:c.1019T>C, NM_001166504.2:c.1043T>C, NM_001166504.1:c.1043T>C, NP_000664.3:p.Val328Ala, NP_001159976.1:p.Val348Ala

Select item 14904548956.

rs1490454895 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:99416538 (GRCh38)
4:100337695 (GRCh37)
Canonical SPDI:: NC_000004.12:99416537:T:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.99416538T>C, NC_000004.11:g.100337695T>C

Select item 14904010767.

rs1490401076 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 14903401068.

rs1490340106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 4:99423650 (GRCh38)
4:100344807 (GRCh37)
Canonical SPDI:: NC_000004.12:99423649:A:C,NC_000004.12:99423649:A:G
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000342/1 (KOREAN)
HGVS:: NC_000004.12:g.99423650A>C, NC_000004.12:g.99423650A>G, NC_000004.11:g.100344807A>C, NC_000004.11:g.100344807A>G

Select item 14901874249.

rs1490187424 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 4:99415355 (GRCh38)
4:100336513 (GRCh37)
Canonical SPDI:: NC_000004.12:99415355:T:TT
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.99415356dup, NC_000004.11:g.100336513dup

Select item 149010032010.

rs1490100320 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:99418063 (GRCh38)
4:100339220 (GRCh37)
Canonical SPDI:: NC_000004.12:99418062:G:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.99418063G>A, NC_000004.11:g.100339220G>A

Select item 149007291311.

rs1490072913 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:99430242 (GRCh38)
4:100351399 (GRCh37)
Canonical SPDI:: NC_000004.12:99430241:C:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000004.12:g.99430242C>A, NC_000004.11:g.100351399C>A

Select item 148998041912.

rs1489980419 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:99420350 (GRCh38)
4:100341507 (GRCh37)
Canonical SPDI:: NC_000004.12:99420349:C:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000671/3 (ALFA)
A=0.000021/3 (GnomAD)
A=0.00067/3 (Estonian)
HGVS:: NC_000004.12:g.99420350C>A, NC_000004.11:g.100341507C>A

Select item 148994474213.

rs1489944742 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:99422109 (GRCh38)
4:100343266 (GRCh37)
Canonical SPDI:: NC_000004.12:99422108:T:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000108/2 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000004.12:g.99422109T>C, NC_000004.11:g.100343266T>C

Select item 148994288414.

rs1489942884 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:99417676 (GRCh38)
4:100338833 (GRCh37)
Canonical SPDI:: NC_000004.12:99417675:G:T
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.99417676G>T, NC_000004.11:g.100338833G>T

Select item 148992551615.

rs1489925516 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:99429828 (GRCh38)
4:100350985 (GRCh37)
Canonical SPDI:: NC_000004.12:99429827:C:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000004.12:g.99429828C>A, NC_000004.11:g.100350985C>A

Select item 148978588416.

rs1489785884 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:99431304 (GRCh38)
4:100352461 (GRCh37)
Canonical SPDI:: NC_000004.12:99431303:A:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.99431304A>C, NC_000004.11:g.100352461A>C

Select item 148969850517.

rs1489698505 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:99427263 (GRCh38)
4:100348420 (GRCh37)
Canonical SPDI:: NC_000004.12:99427262:G:A,NC_000004.12:99427262:G:C
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000035/1 (TOMMO)
A=0.000045/12 (TOPMED)
A=0.000057/8 (GnomAD)
HGVS:: NC_000004.12:g.99427263G>A, NC_000004.12:g.99427263G>C, NC_000004.11:g.100348420G>A, NC_000004.11:g.100348420G>C

Select item 148957050718.

rs1489570507 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 4:99422493 (GRCh38)
4:100343650 (GRCh37)
Canonical SPDI:: NC_000004.12:99422492:GGG:GG
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.99422495del, NC_000004.11:g.100343652del

Select item 148930578319.

rs1489305783 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:99421290 (GRCh38)
4:100342447 (GRCh37)
Canonical SPDI:: NC_000004.12:99421289:T:A
Gene:: ADH7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.99421290T>A, NC_000004.11:g.100342447T>A

Select item 148920227920.

rs1489202279 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:99414593 (GRCh38)
4:100335750 (GRCh37)
Canonical SPDI:: NC_000004.12:99414592:C:A
Gene:: ADH7 (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_000004.12:g.99414593C>A, NC_000004.11:g.100335750C>A

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