SNP Links for Gene (Select 100505933) - SNP

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Select item 14915622201.

rs1491562220 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 10:109964980 (GRCh38)
10:111724738 (GRCh37)
Canonical SPDI:: NC_000010.11:109964979:TG:
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000010.11:g.109964980_109964981del, NC_000010.10:g.111724738_111724739del

Select item 14915521952.

rs1491552195 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 10:110003303 (GRCh38)
10:111763062 (GRCh37)
Canonical SPDI:: NC_000010.11:110003303:T:TCT
Gene:: ADD3 (Varview), ADD3-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000010.11:g.110003304_110003305insCT, NC_000010.10:g.111763062_111763063insCT, NG_051033.1:g.11955_11956insCT

Select item 14915404003.

rs1491540400 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 10:109992487 (GRCh38)
10:111752245 (GRCh37)
Canonical SPDI:: NC_000010.11:109992486:GT:
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.109992487_109992488del, NC_000010.10:g.111752245_111752246del, NG_051033.1:g.1138_1139del

Select item 14914932114.

rs1491493211 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 10:109974559 (GRCh38)
10:111734318 (GRCh37)
Canonical SPDI:: NC_000010.11:109974559::C
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000927/11 (ALFA)
C=0.001459/155 (GnomAD)
HGVS:: NC_000010.11:g.109974559_109974560insC, NC_000010.10:g.111734317_111734318insC

Select item 14914760625.

rs1491476062 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TT [Show Flanks]
Chromosome:: 10:109992487 (GRCh38)
10:111752246 (GRCh37)
Canonical SPDI:: NC_000010.11:109992487:T:TTT
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0./0 (ALFA)
TT=0.000004/1 (TOPMED)
TT=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.109992488_109992489insTT, NC_000010.10:g.111752246_111752247insTT, NG_051033.1:g.1139_1140insTT

Select item 14914736936.

rs1491473693 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CACACACACACAC,CACACACACACACAC [Show Flanks]
Chromosome:: 10:109957979 (GRCh38)
10:111717738 (GRCh37)
Canonical SPDI:: NC_000010.11:109957979:C:CCACACACACACAC,NC_000010.11:109957979:C:CCACACACACACACAC
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000010.11:g.109957980_109957981insCACACACACACAC, NC_000010.11:g.109957980_109957981insCACACACACACACAC, NC_000010.10:g.111717738_111717739insCACACACACACAC, NC_000010.10:g.111717738_111717739insCACACACACACACAC

Select item 14913293417.

rs1491329341 has merged into rs1224675429 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: 10:109961381 (GRCh38)
10:111721139 (GRCh37)
Canonical SPDI:: NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000010.11:109961368:TGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTG=0./0 (ALFA)
TG=0.10483/525 (1000Genomes)
TGTG=0.125/1 (KOREAN)
HGVS:: NC_000010.11:g.109961369TG[6], NC_000010.11:g.109961369TG[7], NC_000010.11:g.109961369TG[8], NC_000010.11:g.109961369TG[9], NC_000010.11:g.109961369TG[10], NC_000010.11:g.109961369TG[11], NC_000010.11:g.109961369TG[12], NC_000010.11:g.109961369TG[14], NC_000010.11:g.109961369TG[15], NC_000010.11:g.109961369TG[16], NC_000010.11:g.109961369TG[17], NC_000010.11:g.109961369TG[18], NC_000010.10:g.111721127TG[6], NC_000010.10:g.111721127TG[7], NC_000010.10:g.111721127TG[8], NC_000010.10:g.111721127TG[9], NC_000010.10:g.111721127TG[10], NC_000010.10:g.111721127TG[11], NC_000010.10:g.111721127TG[12], NC_000010.10:g.111721127TG[14], NC_000010.10:g.111721127TG[15], NC_000010.10:g.111721127TG[16], NC_000010.10:g.111721127TG[17], NC_000010.10:g.111721127TG[18]

Select item 14912801458.

rs1491280145 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTTATTTTA [Show Flanks]
Chromosome:: 10:109983321 (GRCh38)
10:111743080 (GRCh37)
Canonical SPDI:: NC_000010.11:109983321:TTTATTTTA:TTTATTTTACTTTATTTTA
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTATTTTACTTTATTTTA=0./0 (ALFA)
TTTATTTTAC=0.000004/1 (TOPMED)
TTTATTTTAC=0.000017/2 (GnomAD)
HGVS:: NC_000010.11:g.109983330_109983331insCTTTATTTTA, NC_000010.10:g.111743088_111743089insCTTTATTTTA

Select item 14912633479.

rs1491263347 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 10:109964980 (GRCh38)
10:111724739 (GRCh37)
Canonical SPDI:: NC_000010.11:109964980:G:GG
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000010.11:g.109964981dup, NC_000010.10:g.111724739dup

Select item 149123127010.

rs1491231270 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 10:109983323 (GRCh38)
10:111743081 (GRCh37)
Canonical SPDI:: NC_000010.11:109983320:TTTT:TT
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.109983323_109983324del, NC_000010.10:g.111743081_111743082del

Select item 149115956311.

rs1491159563 has merged into rs57236790 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:109974569 (GRCh38)
10:111734327 (GRCh37)
Canonical SPDI:: NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:109974558:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.109974569_109974584del, NC_000010.11:g.109974570_109974584del, NC_000010.11:g.109974571_109974584del, NC_000010.11:g.109974572_109974584del, NC_000010.11:g.109974573_109974584del, NC_000010.11:g.109974574_109974584del, NC_000010.11:g.109974575_109974584del, NC_000010.11:g.109974576_109974584del, NC_000010.11:g.109974577_109974584del, NC_000010.11:g.109974578_109974584del, NC_000010.11:g.109974579_109974584del, NC_000010.11:g.109974580_109974584del, NC_000010.11:g.109974581_109974584del, NC_000010.11:g.109974582_109974584del, NC_000010.11:g.109974583_109974584del, NC_000010.11:g.109974584del, NC_000010.11:g.109974584dup, NC_000010.11:g.109974583_109974584dup, NC_000010.11:g.109974582_109974584dup, NC_000010.11:g.109974581_109974584dup, NC_000010.11:g.109974580_109974584dup, NC_000010.11:g.109974579_109974584dup, NC_000010.11:g.109974578_109974584dup, NC_000010.11:g.109974572_109974584dup, NC_000010.11:g.109974584_109974585insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.111734327_111734342del, NC_000010.10:g.111734328_111734342del, NC_000010.10:g.111734329_111734342del, NC_000010.10:g.111734330_111734342del, NC_000010.10:g.111734331_111734342del, NC_000010.10:g.111734332_111734342del, NC_000010.10:g.111734333_111734342del, NC_000010.10:g.111734334_111734342del, NC_000010.10:g.111734335_111734342del, NC_000010.10:g.111734336_111734342del, NC_000010.10:g.111734337_111734342del, NC_000010.10:g.111734338_111734342del, NC_000010.10:g.111734339_111734342del, NC_000010.10:g.111734340_111734342del, NC_000010.10:g.111734341_111734342del, NC_000010.10:g.111734342del, NC_000010.10:g.111734342dup, NC_000010.10:g.111734341_111734342dup, NC_000010.10:g.111734340_111734342dup, NC_000010.10:g.111734339_111734342dup, NC_000010.10:g.111734338_111734342dup, NC_000010.10:g.111734337_111734342dup, NC_000010.10:g.111734336_111734342dup, NC_000010.10:g.111734330_111734342dup, NC_000010.10:g.111734342_111734343insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149109205612.

rs1491092056 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACACACACACACACACACACACACACCC,ACACACACACACACACACACACACCC,ACACACACACACACACACACCC,ACACACACACACACACACCC,ACACACACACACACACCC,ACACACACACACACCC,ACACACACACACCC,ACACACACACCC,ACACACACCC,ACACACACCCCC,ACACACCC [Show Flanks]
Chromosome:: 10:109957997 (GRCh38)
10:111717756 (GRCh37)
Canonical SPDI:: NC_000010.11:109957997:C:CACACACACACACACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACACCC,NC_000010.11:109957997:C:CACACACACACACCC,NC_000010.11:109957997:C:CACACACACACCC,NC_000010.11:109957997:C:CACACACACCC,NC_000010.11:109957997:C:CACACACACCCCC,NC_000010.11:109957997:C:CACACACCC
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACACACCC=0./0 (ALFA)
CACACACC=0.000004/1 (TOPMED)
CACACACACACC=0.000142/2 (TOMMO)
HGVS:: NC_000010.11:g.109957998CA[13]CCC[1], NC_000010.11:g.109957998CA[12]CCC[1], NC_000010.11:g.109957998CA[10]CCC[1], NC_000010.11:g.109957998CA[9]CCC[1], NC_000010.11:g.109957998CA[8]CCC[1], NC_000010.11:g.109957998CA[7]CCC[1], NC_000010.11:g.109957998CA[6]CCC[1], NC_000010.11:g.109957998CA[5]CCC[1], NC_000010.11:g.109957998CA[4]CCC[1], NC_000010.11:g.109957998CA[4]C[5], NC_000010.11:g.109957998CA[3]CCC[1], NC_000010.10:g.111717756CA[13]CCC[1], NC_000010.10:g.111717756CA[12]CCC[1], NC_000010.10:g.111717756CA[10]CCC[1], NC_000010.10:g.111717756CA[9]CCC[1], NC_000010.10:g.111717756CA[8]CCC[1], NC_000010.10:g.111717756CA[7]CCC[1], NC_000010.10:g.111717756CA[6]CCC[1], NC_000010.10:g.111717756CA[5]CCC[1], NC_000010.10:g.111717756CA[4]CCC[1], NC_000010.10:g.111717756CA[4]C[5], NC_000010.10:g.111717756CA[3]CCC[1]

Select item 149106543113.

rs1491065431 has merged into rs1460611599 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>-,AGAG [Show Flanks]
Chromosome:: 10:109961395 (GRCh38)
10:111721153 (GRCh37)
Canonical SPDI:: NC_000010.11:109961393:GAG:G,NC_000010.11:109961393:GAG:GAGAG
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAG=0./0 (ALFA)
GA=0.000004/1 (TOPMED)
-=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.109961395_109961396del, NC_000010.11:g.109961395_109961396dup, NC_000010.10:g.111721153_111721154del, NC_000010.10:g.111721153_111721154dup

Select item 149104375714.

rs1491043757 has merged into rs57999730 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 10:109975222 (GRCh38)
10:111734980 (GRCh37)
Canonical SPDI:: NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:109975209:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.095/57 (NorthernSweden)
T=0.1/4 (GENOME_DK)
T=0.33307/1668 (1000Genomes)
HGVS:: NC_000010.11:g.109975222_109975223del, NC_000010.11:g.109975223del, NC_000010.11:g.109975223dup, NC_000010.11:g.109975222_109975223dup, NC_000010.11:g.109975221_109975223dup, NC_000010.11:g.109975220_109975223dup, NC_000010.10:g.111734980_111734981del, NC_000010.10:g.111734981del, NC_000010.10:g.111734981dup, NC_000010.10:g.111734980_111734981dup, NC_000010.10:g.111734979_111734981dup, NC_000010.10:g.111734978_111734981dup

Select item 149094918915.

rs1490949189 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:110004539 (GRCh38)
10:111764297 (GRCh37)
Canonical SPDI:: NC_000010.11:110004538:G:C
Gene:: ADD3 (Varview), ADD3-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.110004539G>C, NC_000010.10:g.111764297G>C, NG_051033.1:g.13190G>C

Select item 149091249416.

rs1490912494 has merged into rs950753021 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAAACAAACAAA>-,CAAA,CAAACAAA,CAAACAAACAAACAAA [Show Flanks]
Chromosome:: 10:109952615 (GRCh38)
10:111712373 (GRCh37)
Canonical SPDI:: NC_000010.11:109952603:AAACAAACAAACAAACAAACAAA:AAACAAACAAA,NC_000010.11:109952603:AAACAAACAAACAAACAAACAAA:AAACAAACAAACAAA,NC_000010.11:109952603:AAACAAACAAACAAACAAACAAA:AAACAAACAAACAAACAAA,NC_000010.11:109952603:AAACAAACAAACAAACAAACAAA:AAACAAACAAACAAACAAACAAACAAA
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAACAAACAAACAAA=0./0 (ALFA)
-=0.00007/1 (TOMMO)
-=0.00022/1 (Estonian)
-=0.00156/10 (1000Genomes)
HGVS:: NC_000010.11:g.109952607CAAA[2], NC_000010.11:g.109952607CAAA[3], NC_000010.11:g.109952607CAAA[4], NC_000010.11:g.109952607CAAA[6], NC_000010.10:g.111712365CAAA[2], NC_000010.10:g.111712365CAAA[3], NC_000010.10:g.111712365CAAA[4], NC_000010.10:g.111712365CAAA[6]

Select item 149090329717.

rs1490903297 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:110000206 (GRCh38)
10:111759964 (GRCh37)
Canonical SPDI:: NC_000010.11:110000205:C:G
Gene:: ADD3 (Varview), ADD3-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.110000206C>G, NC_000010.10:g.111759964C>G, NG_051033.1:g.8857C>G

Select item 149090024518.

rs1490900245 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:109967497 (GRCh38)
10:111727255 (GRCh37)
Canonical SPDI:: NC_000010.11:109967496:G:A,NC_000010.11:109967496:G:C
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000142/2 (TOMMO)
HGVS:: NC_000010.11:g.109967497G>A, NC_000010.11:g.109967497G>C, NC_000010.10:g.111727255G>A, NC_000010.10:g.111727255G>C

Select item 149087506019.

rs1490875060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:109968734 (GRCh38)
10:111728492 (GRCh37)
Canonical SPDI:: NC_000010.11:109968733:A:G
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.109968734A>G, NC_000010.10:g.111728492A>G

Select item 149080976020.

rs1490809760 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:109960914 (GRCh38)
10:111720672 (GRCh37)
Canonical SPDI:: NC_000010.11:109960913:T:C
Gene:: ADD3-AS1 (Varview)
Functional Consequence:: intron_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_000010.11:g.109960914T>C, NC_000010.10:g.111720672T>C

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