SNP Links for Gene (Select 693228) - SNP

Links from Gene

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Select item 14915824661.

rs1491582466 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 19:52282034 (GRCh38)
19:52785288 (GRCh37)
Canonical SPDI:: NC_000019.10:52282034:A:AA
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000142/2 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.52282035dup, NC_000019.9:g.52785288dup

Select item 14913905082.

rs1491390508 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 19:52281166 (GRCh38)
19:52784420 (GRCh37)
Canonical SPDI:: NC_000019.10:52281166::T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,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_000019.10:g.52281166_52281167insT, NC_000019.9:g.52784419_52784420insT

Select item 14912535003.

rs1491253500 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 19:52282034 (GRCh38)
19:52785287 (GRCh37)
Canonical SPDI:: NC_000019.10:52282033:TA:
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.52282034_52282035del, NC_000019.9:g.52785287_52785288del

Select item 14899497684.

rs1489949768 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:52280669 (GRCh38)
19:52783922 (GRCh37)
Canonical SPDI:: NC_000019.10:52280668:G:A
Gene:: ZNF766 (Varview), MIR643 (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=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.52280669G>A, NC_000019.9:g.52783922G>A

Select item 14886468555.

rs1488646855 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:52281427 (GRCh38)
19:52784680 (GRCh37)
Canonical SPDI:: NC_000019.10:52281426:G:A
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
HGVS:: NC_000019.10:g.52281427G>A, NC_000019.9:g.52784680G>A

Select item 14879630346.

rs1487963034 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:52282008 (GRCh38)
19:52785261 (GRCh37)
Canonical SPDI:: NC_000019.10:52282007:G:A
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_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_000019.10:g.52282008G>A, NC_000019.9:g.52785261G>A

Select item 14860346657.

rs1486034665 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:52280199 (GRCh38)
19:52783452 (GRCh37)
Canonical SPDI:: NC_000019.10:52280198:G:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.52280199G>T, NC_000019.9:g.52783452G>T

Select item 14845689788.

rs1484568978 [Homo sapiens]

Variant type:: SNV:
Alleles:: CAC>-
Chromosome:: no mapping
Canonical SPDI:

Select item 14801095159.

rs1480109515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:52280183 (GRCh38)
19:52783436 (GRCh37)
Canonical SPDI:: NC_000019.10:52280182:G:A
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000019.10:g.52280183G>A, NC_000019.9:g.52783436G>A

Select item 147505730810.

rs1475057308 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:52280405 (GRCh38)
19:52783658 (GRCh37)
Canonical SPDI:: NC_000019.10:52280404:G:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.52280405G>T, NC_000019.9:g.52783658G>T

Select item 147314679311.

rs1473146793 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:52281758 (GRCh38)
19:52785011 (GRCh37)
Canonical SPDI:: NC_000019.10:52281757:C:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.52281758C>T, NC_000019.9:g.52785011C>T

Select item 147226163312.

rs1472261633 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:52279830 (GRCh38)
19:52783083 (GRCh37)
Canonical SPDI:: NC_000019.10:52279829:C:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: T=0.00018/3 (TOMMO)
HGVS:: NC_000019.10:g.52279830C>T, NC_000019.9:g.52783083C>T

Select item 147127472113.

rs1471274721 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:52281546 (GRCh38)
19:52784799 (GRCh37)
Canonical SPDI:: NC_000019.10:52281545:C:A,NC_000019.10:52281545:C:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.52281546C>A, NC_000019.10:g.52281546C>T, NC_000019.9:g.52784799C>A, NC_000019.9:g.52784799C>T

Select item 147117669314.

rs1471176693 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:52280895 (GRCh38)
19:52784148 (GRCh37)
Canonical SPDI:: NC_000019.10:52280894:C:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.52280895C>T, NC_000019.9:g.52784148C>T

Select item 146907444915.

rs1469074449 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:52281850 (GRCh38)
19:52785103 (GRCh37)
Canonical SPDI:: NC_000019.10:52281849:C:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.52281850C>T, NC_000019.9:g.52785103C>T, NR_030373.1:n.54C>T

Select item 146759691716.

rs1467596917 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:52280985 (GRCh38)
19:52784238 (GRCh37)
Canonical SPDI:: NC_000019.10:52280984:A:G
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000019.10:g.52280985A>G, NC_000019.9:g.52784238A>G

Select item 146734808917.

rs1467348089 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:52281388 (GRCh38)
19:52784641 (GRCh37)
Canonical SPDI:: NC_000019.10:52281387:G:A,NC_000019.10:52281387:G:T
Gene:: ZNF766 (Varview), MIR643 (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./0 (GnomAD)
A=0.000076/1 (GnomAD_exomes)
A=0.000212/6 (TOMMO)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000019.10:g.52281388G>A, NC_000019.10:g.52281388G>T, NC_000019.9:g.52784641G>A, NC_000019.9:g.52784641G>T

Select item 146687867818.

rs1466878678 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:52281851 (GRCh38)
19:52785104 (GRCh37)
Canonical SPDI:: NC_000019.10:52281850:A:T
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000019.10:g.52281851A>T, NC_000019.9:g.52785104A>T, NR_030373.1:n.55A>T

Select item 146668312819.

rs1466683128 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:52279897 (GRCh38)
19:52783150 (GRCh37)
Canonical SPDI:: NC_000019.10:52279896:A:G
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000022/3 (GnomAD)
HGVS:: NC_000019.10:g.52279897A>G, NC_000019.9:g.52783150A>G

Select item 146491748720.

rs1464917487 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:52282014 (GRCh38)
19:52785267 (GRCh37)
Canonical SPDI:: NC_000019.10:52282013:A:G
Gene:: ZNF766 (Varview), MIR643 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_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_000019.10:g.52282014A>G, NC_000019.9:g.52785267A>G

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