SNP Links for Gene (Select 10344) - SNP

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Select item 14913447441.

rs1491344744 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 7:75789096 (GRCh38)
7:75418414 (GRCh37)
Canonical SPDI:: NC_000007.14:75789095:AT:
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000007.14:g.75789096_75789097del, NC_000007.13:g.75418414_75418415del, NG_015989.1:g.5650_5651del, NW_003871064.1:g.3318332_3318333del

Select item 14913279682.

rs1491327968 has merged into rs527793902 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:75789109 (GRCh38)
7:75418427 (GRCh37)
Canonical SPDI:: NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.2977/1491 (1000Genomes)
HGVS:: NC_000007.14:g.75789109_75789113del, NC_000007.14:g.75789110_75789113del, NC_000007.14:g.75789111_75789113del, NC_000007.14:g.75789112_75789113del, NC_000007.14:g.75789113del, NC_000007.14:g.75789113dup, NC_000007.14:g.75789112_75789113dup, NC_000007.14:g.75789111_75789113dup, NC_000007.14:g.75789110_75789113dup, NC_000007.14:g.75789109_75789113dup, NC_000007.14:g.75789108_75789113dup, NC_000007.14:g.75789107_75789113dup, NC_000007.14:g.75789106_75789113dup, NC_000007.14:g.75789105_75789113dup, NC_000007.14:g.75789103_75789113dup, NC_000007.13:g.75418427_75418431del, NC_000007.13:g.75418428_75418431del, NC_000007.13:g.75418429_75418431del, NC_000007.13:g.75418430_75418431del, NC_000007.13:g.75418431del, NC_000007.13:g.75418431dup, NC_000007.13:g.75418430_75418431dup, NC_000007.13:g.75418429_75418431dup, NC_000007.13:g.75418428_75418431dup, NC_000007.13:g.75418427_75418431dup, NC_000007.13:g.75418426_75418431dup, NC_000007.13:g.75418425_75418431dup, NC_000007.13:g.75418424_75418431dup, NC_000007.13:g.75418423_75418431dup, NC_000007.13:g.75418421_75418431dup, NG_015989.1:g.5646_5650del, NG_015989.1:g.5647_5650del, NG_015989.1:g.5648_5650del, NG_015989.1:g.5649_5650del, NG_015989.1:g.5650del, NG_015989.1:g.5650dup, NG_015989.1:g.5649_5650dup, NG_015989.1:g.5648_5650dup, NG_015989.1:g.5647_5650dup, NG_015989.1:g.5646_5650dup, NG_015989.1:g.5645_5650dup, NG_015989.1:g.5644_5650dup, NG_015989.1:g.5643_5650dup, NG_015989.1:g.5642_5650dup, NG_015989.1:g.5640_5650dup, NW_003871064.1:g.3318345_3318349del, NW_003871064.1:g.3318346_3318349del, NW_003871064.1:g.3318347_3318349del, NW_003871064.1:g.3318348_3318349del, NW_003871064.1:g.3318349del, NW_003871064.1:g.3318349dup, NW_003871064.1:g.3318348_3318349dup, NW_003871064.1:g.3318347_3318349dup, NW_003871064.1:g.3318346_3318349dup, NW_003871064.1:g.3318345_3318349dup, NW_003871064.1:g.3318344_3318349dup, NW_003871064.1:g.3318343_3318349dup, NW_003871064.1:g.3318342_3318349dup, NW_003871064.1:g.3318341_3318349dup, NW_003871064.1:g.3318339_3318349dup

Select item 14910673633.

rs1491067363 has merged into rs527793902 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:75789109 (GRCh38)
7:75418427 (GRCh37)
Canonical SPDI:: NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:75789096:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.2977/1491 (1000Genomes)
HGVS:: NC_000007.14:g.75789109_75789113del, NC_000007.14:g.75789110_75789113del, NC_000007.14:g.75789111_75789113del, NC_000007.14:g.75789112_75789113del, NC_000007.14:g.75789113del, NC_000007.14:g.75789113dup, NC_000007.14:g.75789112_75789113dup, NC_000007.14:g.75789111_75789113dup, NC_000007.14:g.75789110_75789113dup, NC_000007.14:g.75789109_75789113dup, NC_000007.14:g.75789108_75789113dup, NC_000007.14:g.75789107_75789113dup, NC_000007.14:g.75789106_75789113dup, NC_000007.14:g.75789105_75789113dup, NC_000007.14:g.75789103_75789113dup, NC_000007.13:g.75418427_75418431del, NC_000007.13:g.75418428_75418431del, NC_000007.13:g.75418429_75418431del, NC_000007.13:g.75418430_75418431del, NC_000007.13:g.75418431del, NC_000007.13:g.75418431dup, NC_000007.13:g.75418430_75418431dup, NC_000007.13:g.75418429_75418431dup, NC_000007.13:g.75418428_75418431dup, NC_000007.13:g.75418427_75418431dup, NC_000007.13:g.75418426_75418431dup, NC_000007.13:g.75418425_75418431dup, NC_000007.13:g.75418424_75418431dup, NC_000007.13:g.75418423_75418431dup, NC_000007.13:g.75418421_75418431dup, NG_015989.1:g.5646_5650del, NG_015989.1:g.5647_5650del, NG_015989.1:g.5648_5650del, NG_015989.1:g.5649_5650del, NG_015989.1:g.5650del, NG_015989.1:g.5650dup, NG_015989.1:g.5649_5650dup, NG_015989.1:g.5648_5650dup, NG_015989.1:g.5647_5650dup, NG_015989.1:g.5646_5650dup, NG_015989.1:g.5645_5650dup, NG_015989.1:g.5644_5650dup, NG_015989.1:g.5643_5650dup, NG_015989.1:g.5642_5650dup, NG_015989.1:g.5640_5650dup, NW_003871064.1:g.3318345_3318349del, NW_003871064.1:g.3318346_3318349del, NW_003871064.1:g.3318347_3318349del, NW_003871064.1:g.3318348_3318349del, NW_003871064.1:g.3318349del, NW_003871064.1:g.3318349dup, NW_003871064.1:g.3318348_3318349dup, NW_003871064.1:g.3318347_3318349dup, NW_003871064.1:g.3318346_3318349dup, NW_003871064.1:g.3318345_3318349dup, NW_003871064.1:g.3318344_3318349dup, NW_003871064.1:g.3318343_3318349dup, NW_003871064.1:g.3318342_3318349dup, NW_003871064.1:g.3318341_3318349dup, NW_003871064.1:g.3318339_3318349dup

Select item 14909254374.

rs1490925437 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:75789114 (GRCh38)
7:75418432 (GRCh37)
Canonical SPDI:: NC_000007.14:75789113:G:A,NC_000007.14:75789113:G:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00356/59 (TOMMO)
T=0.00659/12 (Korea1K)
T=0.13853/402 (KOREAN)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000007.14:g.75789114G>A, NC_000007.14:g.75789114G>T, NC_000007.13:g.75418432G>A, NC_000007.13:g.75418432G>T, NG_015989.1:g.5633C>T, NG_015989.1:g.5633C>A, NW_003871064.1:g.3318350G>A, NW_003871064.1:g.3318350G>T

Select item 14908316155.

rs1490831615 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:75775059 (GRCh38)
7:75404377 (GRCh37)
Canonical SPDI:: NC_000007.14:75775058:A:C
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00003/8 (TOPMED)
C=0.000043/6 (GnomAD)
HGVS:: NC_000007.14:g.75775059A>C, NC_000007.13:g.75404377A>C, NG_015989.1:g.19688T>G, NW_003871064.1:g.3304295A>C

Select item 14903264156.

rs1490326415 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:75783332 (GRCh38)
7:75412650 (GRCh37)
Canonical SPDI:: NC_000007.14:75783331:C:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000021/3 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.75783332C>T, NC_000007.13:g.75412650C>T, NG_015989.1:g.11415G>A, NW_003871064.1:g.3312568C>T

Select item 14902975107.

rs1490297510 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:75782212 (GRCh38)
7:75411530 (GRCh37)
Canonical SPDI:: NC_000007.14:75782211:A:G
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.75782212A>G, NC_000007.13:g.75411530A>G, NG_015989.1:g.12535T>C, NW_003871064.1:g.3311448A>G

Select item 14902727998.

rs1490272799 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:75769220 (GRCh38)
7:75398538 (GRCh37)
Canonical SPDI:: NC_000007.14:75769219:G:A
Gene:: CCL26 (Varview)
Functional Consequence:: downstream_transcript_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_000007.14:g.75769220G>A, NC_000007.13:g.75398538G>A, NG_015989.1:g.25527C>T, NW_003871064.1:g.3298456G>A

Select item 14901086679.

rs1490108667 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:75789445 (GRCh38)
7:75418763 (GRCh37)
Canonical SPDI:: NC_000007.14:75789444:C:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000277/4 (ALFA)
T=0.000113/15 (GnomAD)
T=0.000132/35 (TOPMED)
HGVS:: NC_000007.14:g.75789445C>T, NC_000007.13:g.75418763C>T, NG_015989.1:g.5302G>A, NW_003871064.1:g.3318681C>T

Select item 149009385310.

rs1490093853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:75788721 (GRCh38)
7:75418039 (GRCh37)
Canonical SPDI:: NC_000007.14:75788720:G:A
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000037/5 (GnomAD)
A=0.000106/2 (TOMMO)
A=0.001712/5 (KOREAN)
HGVS:: NC_000007.14:g.75788721G>A, NC_000007.13:g.75418039G>A, NG_015989.1:g.6026C>T, NW_003871064.1:g.3317957G>A

Select item 149006764611.

rs1490067646 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:75776394 (GRCh38)
7:75405712 (GRCh37)
Canonical SPDI:: NC_000007.14:75776393:G:A
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.75776394G>A, NC_000007.13:g.75405712G>A, NG_015989.1:g.18353C>T, NW_003871064.1:g.3305630G>A

Select item 149001487812.

rs1490014878 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:75775595 (GRCh38)
7:75404913 (GRCh37)
Canonical SPDI:: NC_000007.14:75775594:G:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.75775595G>T, NC_000007.13:g.75404913G>T, NG_015989.1:g.19152C>A, NW_003871064.1:g.3304831G>T

Select item 148983172913.

rs1489831729 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:75782778 (GRCh38)
7:75412096 (GRCh37)
Canonical SPDI:: NC_000007.14:75782777:A:G
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_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_000007.14:g.75782778A>G, NC_000007.13:g.75412096A>G, NG_015989.1:g.11969T>C, NW_003871064.1:g.3312014A>G

Select item 148966083314.

rs1489660833 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:75777714 (GRCh38)
7:75407032 (GRCh37)
Canonical SPDI:: NC_000007.14:75777713:T:C
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.75777714T>C, NC_000007.13:g.75407032T>C, NG_015989.1:g.17033A>G, NW_003871064.1:g.3306950T>C

Select item 148960842315.

rs1489608423 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:75776754 (GRCh38)
7:75406072 (GRCh37)
Canonical SPDI:: NC_000007.14:75776753:C:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.00005/7 (GnomAD)
T=0.000098/26 (TOPMED)
HGVS:: NC_000007.14:g.75776754C>T, NC_000007.13:g.75406072C>T, NG_015989.1:g.17993G>A, NW_003871064.1:g.3305990C>T

Select item 148958007916.

rs1489580079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:75793578 (GRCh38)
7:75422896 (GRCh37)
Canonical SPDI:: NC_000007.14:75793577:G:A,NC_000007.14:75793577:G:C
Gene:: CCL26 (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=0.000023/6 (TOPMED)
C=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.75793578G>A, NC_000007.14:g.75793578G>C, NC_000007.13:g.75422896G>A, NC_000007.13:g.75422896G>C, NG_015989.1:g.1169C>T, NG_015989.1:g.1169C>G, NW_003871064.1:g.3322814G>A, NW_003871064.1:g.3322814G>C

Select item 148954924117.

rs1489549241 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATAAGTAA [Show Flanks]
Chromosome:: 7:75792788 (GRCh38)
7:75422107 (GRCh37)
Canonical SPDI:: NC_000007.14:75792788:TAA:TAAATAAGTAA
Gene:: CCL26 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TAAATAAGTAA=0.000084/1 (ALFA)
TAAATAAG=0.000008/1 (GnomAD)
HGVS:: NC_000007.14:g.75792791_75792792insATAAGTAA, NC_000007.13:g.75422109_75422110insATAAGTAA, NG_015989.1:g.1958_1959insCTTATTTA, NW_003871064.1:g.3322027_3322028insATAAGTAA

Select item 148950481418.

rs1489504814 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:75780623 (GRCh38)
7:75409941 (GRCh37)
Canonical SPDI:: NC_000007.14:75780622:G:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.75780623G>T, NC_000007.13:g.75409941G>T, NG_015989.1:g.14124C>A, NW_003871064.1:g.3309859G>T

Select item 148945273519.

rs1489452735 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:75779689 (GRCh38)
7:75409007 (GRCh37)
Canonical SPDI:: NC_000007.14:75779688:C:A,NC_000007.14:75779688:C:T
Gene:: CCL26 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.75779689C>A, NC_000007.14:g.75779689C>T, NC_000007.13:g.75409007C>A, NC_000007.13:g.75409007C>T, NG_015989.1:g.15058G>T, NG_015989.1:g.15058G>A, NW_003871064.1:g.3308925C>A, NW_003871064.1:g.3308925C>T

Select item 148934170020.

rs1489341700 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:75773036 (GRCh38)
7:75402354 (GRCh37)
Canonical SPDI:: NC_000007.14:75773035:A:G
Gene:: CCL26 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.75773036A>G, NC_000007.13:g.75402354A>G, NG_015989.1:g.21711T>C, NG_078360.1:g.406A>G, NW_003871064.1:g.3302272A>G

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