SNP Links for Nucleotide (Select 540344610) - SNP

Links from Nucleotide

Items: 1 to 20 of 187

<< First< Prev

Page of 10

Next >Last >>

Select item 14893316321.

rs1489331632 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:90915002 (GRCh38)
11:90648170 (GRCh37)
Canonical SPDI:: NC_000011.10:90915001:T:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.90915002T>A, NC_000011.9:g.90648170T>A, NR_104190.1:n.724T>A

Select item 14853093182.

rs1485309318 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:90801772 (GRCh38)
11:90534940 (GRCh37)
Canonical SPDI:: NC_000011.10:90801771:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000035/1 (TOMMO)
T=0.000684/2 (KOREAN)
HGVS:: NC_000011.10:g.90801772C>T, NC_000011.9:g.90534940C>T, NR_104190.1:n.339C>T

Select item 14842233023.

rs1484223302 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:90602882 (GRCh38)
11:90336050 (GRCh37)
Canonical SPDI:: NC_000011.10:90602881:C:A,NC_000011.10:90602881:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.90602882C>A, NC_000011.10:g.90602882C>T, NC_000011.9:g.90336050C>A, NC_000011.9:g.90336050C>T, NR_104190.1:n.306C>A, NR_104190.1:n.306C>T

Select item 14832405724.

rs1483240572 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:90251295 (GRCh38)
11:89984463 (GRCh37)
Canonical SPDI:: NC_000011.10:90251294:C:A,NC_000011.10:90251294:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.90251295C>A, NC_000011.10:g.90251295C>T, NC_000011.9:g.89984463C>A, NC_000011.9:g.89984463C>T, NW_019805497.1:g.157418C>A, NW_019805497.1:g.157418C>T, NR_104190.1:n.64C>A, NR_104190.1:n.64C>T

Select item 14814644275.

rs1481464427 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:90915046 (GRCh38)
11:90648214 (GRCh37)
Canonical SPDI:: NC_000011.10:90915045:A:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_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_000011.10:g.90915046A>T, NC_000011.9:g.90648214A>T, NR_104190.1:n.768A>T

Select item 14761743086.

rs1476174308 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:90602813 (GRCh38)
11:90335981 (GRCh37)
Canonical SPDI:: NC_000011.10:90602812:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.90602813C>T, NC_000011.9:g.90335981C>T, NR_104190.1:n.237C>T

Select item 14749697837.

rs1474969783 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:90546825 (GRCh38)
11:90279993 (GRCh37)
Canonical SPDI:: NC_000011.10:90546824:G:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.90546825G>A, NC_000011.9:g.90279993G>A, NR_104190.1:n.158G>A

Select item 14665533628.

rs1466553362 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:90546821 (GRCh38)
11:90279989 (GRCh37)
Canonical SPDI:: NC_000011.10:90546820:A:G
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.90546821A>G, NC_000011.9:g.90279989A>G, NR_104190.1:n.154A>G

Select item 14646440939.

rs1464644093 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:90844890 (GRCh38)
11:90578058 (GRCh37)
Canonical SPDI:: NC_000011.10:90844889:C:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.90844890C>A, NC_000011.9:g.90578058C>A, NR_104190.1:n.440C>A

Select item 146303529510.

rs1463035295 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:90546838 (GRCh38)
11:90280006 (GRCh37)
Canonical SPDI:: NC_000011.10:90546837:T:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.90546838T>A, NC_000011.9:g.90280006T>A, NR_104190.1:n.171T>A

Select item 146181969111.

rs1461819691 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:90844932 (GRCh38)
11:90578100 (GRCh37)
Canonical SPDI:: NC_000011.10:90844931:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.90844932C>T, NC_000011.9:g.90578100C>T, NR_104190.1:n.482C>T

Select item 145743918512.

rs1457439185 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:90852637 (GRCh38)
11:90585805 (GRCh37)
Canonical SPDI:: NC_000011.10:90852636:A:G
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_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.90852637A>G, NC_000011.9:g.90585805A>G, NR_104190.1:n.521A>G

Select item 145740269313.

rs1457402693 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:90546869 (GRCh38)
11:90280037 (GRCh37)
Canonical SPDI:: NC_000011.10:90546868:G:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_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_000011.10:g.90546869G>A, NC_000011.9:g.90280037G>A, NR_104190.1:n.202G>A

Select item 145632996514.

rs1456329965 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:90844886 (GRCh38)
11:90578054 (GRCh37)
Canonical SPDI:: NC_000011.10:90844885:T:C
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.90844886T>C, NC_000011.9:g.90578054T>C, NR_104190.1:n.436T>C

Select item 144541694915.

rs1445416949 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:90914928 (GRCh38)
11:90648096 (GRCh37)
Canonical SPDI:: NC_000011.10:90914927:T:C
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.90914928T>C, NC_000011.9:g.90648096T>C, NR_104190.1:n.650T>C

Select item 144535664516.

rs1445356645 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:90546891 (GRCh38)
11:90280059 (GRCh37)
Canonical SPDI:: NC_000011.10:90546890:T:G
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000011.10:g.90546891T>G, NC_000011.9:g.90280059T>G, NR_104190.1:n.224T>G

Select item 143228745617.

rs1432287456 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:90914964 (GRCh38)
11:90648132 (GRCh37)
Canonical SPDI:: NC_000011.10:90914963:T:C
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_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_000011.10:g.90914964T>C, NC_000011.9:g.90648132T>C, NR_104190.1:n.686T>C

Select item 142753723218.

rs1427537232 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:90602844 (GRCh38)
11:90336012 (GRCh37)
Canonical SPDI:: NC_000011.10:90602843:C:T
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.90602844C>T, NC_000011.9:g.90336012C>T, NR_104190.1:n.268C>T

Select item 142746139319.

rs1427461393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:90915049 (GRCh38)
11:90648217 (GRCh37)
Canonical SPDI:: NC_000011.10:90915048:T:A
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00016/1 (1000Genomes)
A=0.0012/20 (TOMMO)
A=0.00164/3 (Korea1K)
A=0.00513/15 (KOREAN)
HGVS:: NC_000011.10:g.90915049T>A, NC_000011.9:g.90648217T>A, NR_104190.1:n.771T>A

Select item 142455175220.

rs1424551752 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:90915028 (GRCh38)
11:90648196 (GRCh37)
Canonical SPDI:: NC_000011.10:90915027:G:C
Gene:: DISC1FP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.90915028G>C, NC_000011.9:g.90648196G>C, NR_104190.1:n.750G>C

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 187

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity