SNP Links for Gene (Select 171483) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915296691.

rs1491529669 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: X:9126262 (GRCh38)
X:9094304 (GRCh37)
Canonical SPDI:: NC_000023.11:9126262::G
Validated:: by frequency,by alfa
MAF:: G=0.00244/29 (ALFA)
HGVS:: NC_000023.11:g.9126262_9126263insG, NC_000023.10:g.9094303_9094304insG

Select item 14915286832.

rs1491528683 has merged into rs59184046 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACA>-,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA [Show Flanks]
Chromosome:: X:9111670 (GRCh38)
X:9079711 (GRCh37)
Canonical SPDI:: NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000023.11:9111655:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACA=0./0 (ALFA)
CACA=0.36318/1371 (1000Genomes)
HGVS:: NC_000023.11:g.9111656CA[7], NC_000023.11:g.9111656CA[9], NC_000023.11:g.9111656CA[10], NC_000023.11:g.9111656CA[11], NC_000023.11:g.9111656CA[12], NC_000023.11:g.9111656CA[13], NC_000023.11:g.9111656CA[15], NC_000023.11:g.9111656CA[16], NC_000023.11:g.9111656CA[17], NC_000023.11:g.9111656CA[18], NC_000023.11:g.9111656CA[19], NC_000023.11:g.9111656CA[20], NC_000023.10:g.9079697CA[7], NC_000023.10:g.9079697CA[9], NC_000023.10:g.9079697CA[10], NC_000023.10:g.9079697CA[11], NC_000023.10:g.9079697CA[12], NC_000023.10:g.9079697CA[13], NC_000023.10:g.9079697CA[15], NC_000023.10:g.9079697CA[16], NC_000023.10:g.9079697CA[17], NC_000023.10:g.9079697CA[18], NC_000023.10:g.9079697CA[19], NC_000023.10:g.9079697CA[20]

Select item 14915111503.

rs1491511150 has merged into rs762497162 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GAAGAAGAAGAAGG [Show Flanks]
Chromosome:: X:9082389 (GRCh38)
X:9050431 (GRCh37)
Canonical SPDI:: NC_000023.11:9082389:G:GG,NC_000023.11:9082389:G:GGAAGAAGAAGAAGG
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.00593/22 (TWINSUK)
G=0.00762/22 (ALSPAC)
HGVS:: NC_000023.11:g.9082390dup, NC_000023.11:g.9082390_9082391insGAAGAAGAAGAAGG, NC_000023.10:g.9050431dup, NC_000023.10:g.9050431_9050432insGAAGAAGAAGAAGG

Select item 14914888564.

rs1491488856 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: X:9126258 (GRCh38)
X:9094300 (GRCh37)
Canonical SPDI:: NC_000023.11:9126258::G
Validated:: by frequency,by alfa
MAF:: G=0.00008/1 (ALFA)
HGVS:: NC_000023.11:g.9126258_9126259insG, NC_000023.10:g.9094299_9094300insG

Select item 14914500295.

rs1491450029 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTT,CCTTCCTT,CCTTCCTTCCTT,CCTTCCTTCCTTCCTT,CCTTCCTTCCTTCCTTCCTT [Show Flanks]
Chromosome:: X:9115200 (GRCh38)
X:9083242 (GRCh37)
Canonical SPDI:: NC_000023.11:9115200:CTT:CTTCCTT,NC_000023.11:9115200:CTT:CTTCCTTCCTT,NC_000023.11:9115200:CTT:CTTCCTTCCTTCCTT,NC_000023.11:9115200:CTT:CTTCCTTCCTTCCTTCCTT,NC_000023.11:9115200:CTT:CTTCCTTCCTTCCTTCCTTCCTT
Validated:: by frequency,by alfa
MAF:: CTTCCTTCCTT=0./0 (ALFA)
HGVS:: NC_000023.11:g.9115203_9115204insCCTT, NC_000023.11:g.9115203_9115204insCCTTCCTT, NC_000023.11:g.9115204CCTT[3], NC_000023.11:g.9115204CCTT[4], NC_000023.11:g.9115204CCTT[5], NC_000023.10:g.9083244_9083245insCCTT, NC_000023.10:g.9083244_9083245insCCTTCCTT, NC_000023.10:g.9083245CCTT[3], NC_000023.10:g.9083245CCTT[4], NC_000023.10:g.9083245CCTT[5]

Select item 14914352926.

rs1491435292 has merged into rs1156691876 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: X:9116080 (GRCh38)
X:9084121 (GRCh37)
Canonical SPDI:: NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000023.11:9116068:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.00003/8 (TOPMED)
HGVS:: NC_000023.11:g.9116080_9116094del, NC_000023.11:g.9116081_9116094del, NC_000023.11:g.9116082_9116094del, NC_000023.11:g.9116083_9116094del, NC_000023.11:g.9116084_9116094del, NC_000023.11:g.9116085_9116094del, NC_000023.11:g.9116086_9116094del, NC_000023.11:g.9116087_9116094del, NC_000023.11:g.9116088_9116094del, NC_000023.11:g.9116089_9116094del, NC_000023.11:g.9116090_9116094del, NC_000023.11:g.9116091_9116094del, NC_000023.11:g.9116092_9116094del, NC_000023.11:g.9116093_9116094del, NC_000023.11:g.9116094del, NC_000023.11:g.9116094dup, NC_000023.11:g.9116093_9116094dup, NC_000023.11:g.9116092_9116094dup, NC_000023.11:g.9116091_9116094dup, NC_000023.11:g.9116090_9116094dup, NC_000023.10:g.9084121_9084135del, NC_000023.10:g.9084122_9084135del, NC_000023.10:g.9084123_9084135del, NC_000023.10:g.9084124_9084135del, NC_000023.10:g.9084125_9084135del, NC_000023.10:g.9084126_9084135del, NC_000023.10:g.9084127_9084135del, NC_000023.10:g.9084128_9084135del, NC_000023.10:g.9084129_9084135del, NC_000023.10:g.9084130_9084135del, NC_000023.10:g.9084131_9084135del, NC_000023.10:g.9084132_9084135del, NC_000023.10:g.9084133_9084135del, NC_000023.10:g.9084134_9084135del, NC_000023.10:g.9084135del, NC_000023.10:g.9084135dup, NC_000023.10:g.9084134_9084135dup, NC_000023.10:g.9084133_9084135dup, NC_000023.10:g.9084132_9084135dup, NC_000023.10:g.9084131_9084135dup

Select item 14914334447.

rs1491433444 has merged into rs1405602551 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: X:9126259 (GRCh38)
X:9094300 (GRCh37)
Canonical SPDI:: NC_000023.11:9126257:AAA:A,NC_000023.11:9126257:AAA:AA,NC_000023.11:9126257:AAA:AAAA
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.0001/7 (GnomAD)
HGVS:: NC_000023.11:g.9126259_9126260del, NC_000023.11:g.9126260del, NC_000023.11:g.9126260dup, NC_000023.10:g.9094300_9094301del, NC_000023.10:g.9094301del, NC_000023.10:g.9094301dup

Select item 14914209028.

rs1491420902 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: X:9140258 (GRCh38)
X:9108299 (GRCh37)
Canonical SPDI:: NC_000023.11:9140256:ATA:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000015/4 (TOPMED)
-=0.000039/4 (GnomAD)
HGVS:: NC_000023.11:g.9140258_9140259del, NC_000023.10:g.9108299_9108300del

Select item 14914154039.

rs1491415403 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAG [Show Flanks]
Chromosome:: X:9082315 (GRCh38)
X:9050357 (GRCh37)
Canonical SPDI:: NC_000023.11:9082315:AG:AGGAG
Validated:: by frequency,by alfa
MAF:: AGGAG=0./0 (ALFA)
HGVS:: NC_000023.11:g.9082317_9082318insGAG, NC_000023.10:g.9050358_9050359insGAG

Select item 149141023510.

rs1491410235 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TACA [Show Flanks]
Chromosome:: X:9111656 (GRCh38)
X:9079698 (GRCh37)
Canonical SPDI:: NC_000023.11:9111656:ACA:ACATACA
HGVS:: NC_000023.11:g.9111659_9111660insTACA, NC_000023.10:g.9079700_9079701insTACA

Select item 149140582411.

rs1491405824 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: X:9115201 (GRCh38)
X:9083242 (GRCh37)
Canonical SPDI:: NC_000023.11:9115199:TCT:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.9115201_9115202del, NC_000023.10:g.9083242_9083243del

Select item 149139991712.

rs1491399917 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: X:9116068 (GRCh38)
X:9084109 (GRCh37)
Canonical SPDI:: NC_000023.11:9116067:CA:
Validated:: by frequency,by alfa
MAF:: -=0.00287/34 (ALFA)
HGVS:: NC_000023.11:g.9116068_9116069del, NC_000023.10:g.9084109_9084110del

Select item 149139598513.

rs1491395985 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: X:9094153 (GRCh38)
X:9062195 (GRCh37)
Canonical SPDI:: NC_000023.11:9094153::G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.9094153_9094154insG, NC_000023.10:g.9062194_9062195insG

Select item 149138571214.

rs1491385712 has merged into rs1248727219 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>-,GCGC [Show Flanks]
Chromosome:: X:9188872 (GRCh38)
X:9156913 (GRCh37)
Canonical SPDI:: NC_000023.11:9188867:GCGCGC:GCGC,NC_000023.11:9188867:GCGCGC:GCGCGCGC
Validated:: by frequency,by alfa,by cluster
MAF:: GCGCGCGC=0.00076/9 (ALFA)
GC=0.00026/1 (1000Genomes)
-=0.00086/80 (GnomAD)
HGVS:: NC_000023.11:g.9188868GC[2], NC_000023.11:g.9188868GC[4], NC_000023.10:g.9156909GC[2], NC_000023.10:g.9156909GC[4]

Select item 149138152215.

rs1491381522 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: X:9089554 (GRCh38)
X:9057595 (GRCh37)
Canonical SPDI:: NC_000023.11:9089553:TG:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000023.11:g.9089554_9089555del, NC_000023.10:g.9057595_9057596del

Select item 149135172816.

rs1491351728 has merged into rs1259434273 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,TTT,TTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTCCCCCCCTCCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:9104202 (GRCh38)
X:9072243 (GRCh37)
Canonical SPDI:: NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCCCCCCCTCCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:9104192:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000023.11:g.9104202_9104214del, NC_000023.11:g.9104205_9104214del, NC_000023.11:g.9104206_9104214del, NC_000023.11:g.9104209_9104214del, NC_000023.11:g.9104211_9104214del, NC_000023.11:g.9104213_9104214del, NC_000023.11:g.9104214del, NC_000023.11:g.9104214dup, NC_000023.11:g.9104193_9104214T[23]C[7]TCCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000023.11:g.9104213_9104214dup, NC_000023.11:g.9104212_9104214dup, NC_000023.11:g.9104210_9104214dup, NC_000023.11:g.9104209_9104214dup, NC_000023.11:g.9104208_9104214dup, NC_000023.10:g.9072243_9072255del, NC_000023.10:g.9072246_9072255del, NC_000023.10:g.9072247_9072255del, NC_000023.10:g.9072250_9072255del, NC_000023.10:g.9072252_9072255del, NC_000023.10:g.9072254_9072255del, NC_000023.10:g.9072255del, NC_000023.10:g.9072255dup, NC_000023.10:g.9072234_9072255T[23]C[7]TCCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000023.10:g.9072254_9072255dup, NC_000023.10:g.9072253_9072255dup, NC_000023.10:g.9072251_9072255dup, NC_000023.10:g.9072250_9072255dup, NC_000023.10:g.9072249_9072255dup

Select item 149135102817.

rs1491351028 has merged into rs59831938 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAGAGAGAGAGAGAGAGAGAGAGAGAGAG>-,AGAG,AGAGAG,AGAGAGAG,AGAGAGAGAG,AGAGAGAGAGAG,AGAGAGAGAGAGAG,AGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG [Show Flanks]
Chromosome:: X:9089577 (GRCh38)
X:9057618 (GRCh37)
Canonical SPDI:: NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000023.11:9089555:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGAGAGAGAGAGAGAGAGAGAG=0./0 (ALFA)
-=0.0556/206 (TWINSUK)
-=0.0644/186 (ALSPAC)
HGVS:: NC_000023.11:g.9089557AG[10], NC_000023.11:g.9089557AG[12], NC_000023.11:g.9089557AG[13], NC_000023.11:g.9089557AG[14], NC_000023.11:g.9089557AG[15], NC_000023.11:g.9089557AG[16], NC_000023.11:g.9089557AG[17], NC_000023.11:g.9089557AG[18], NC_000023.11:g.9089557AG[19], NC_000023.11:g.9089557AG[20], NC_000023.11:g.9089557AG[21], NC_000023.11:g.9089557AG[22], NC_000023.11:g.9089557AG[23], NC_000023.11:g.9089557AG[24], NC_000023.11:g.9089557AG[26], NC_000023.11:g.9089557AG[27], NC_000023.11:g.9089557AG[28], NC_000023.11:g.9089557AG[29], NC_000023.11:g.9089557AG[30], NC_000023.11:g.9089557AG[31], NC_000023.11:g.9089557AG[32], NC_000023.11:g.9089557AG[33], NC_000023.11:g.9089557AG[34], NC_000023.11:g.9089557AG[35], NC_000023.11:g.9089557AG[36], NC_000023.11:g.9089557AG[37], NC_000023.11:g.9089557AG[38], NC_000023.11:g.9089557AG[39], NC_000023.11:g.9089557AG[40], NC_000023.11:g.9089557AG[41], NC_000023.10:g.9057598AG[10], NC_000023.10:g.9057598AG[12], NC_000023.10:g.9057598AG[13], NC_000023.10:g.9057598AG[14], NC_000023.10:g.9057598AG[15], NC_000023.10:g.9057598AG[16], NC_000023.10:g.9057598AG[17], NC_000023.10:g.9057598AG[18], NC_000023.10:g.9057598AG[19], NC_000023.10:g.9057598AG[20], NC_000023.10:g.9057598AG[21], NC_000023.10:g.9057598AG[22], NC_000023.10:g.9057598AG[23], NC_000023.10:g.9057598AG[24], NC_000023.10:g.9057598AG[26], NC_000023.10:g.9057598AG[27], NC_000023.10:g.9057598AG[28], NC_000023.10:g.9057598AG[29], NC_000023.10:g.9057598AG[30], NC_000023.10:g.9057598AG[31], NC_000023.10:g.9057598AG[32], NC_000023.10:g.9057598AG[33], NC_000023.10:g.9057598AG[34], NC_000023.10:g.9057598AG[35], NC_000023.10:g.9057598AG[36], NC_000023.10:g.9057598AG[37], NC_000023.10:g.9057598AG[38], NC_000023.10:g.9057598AG[39], NC_000023.10:g.9057598AG[40], NC_000023.10:g.9057598AG[41]

Select item 149132157518.

rs1491321575 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AA,AAAA [Show Flanks]
Chromosome:: X:9089556 (GRCh38)
X:9057598 (GRCh37)
Canonical SPDI:: NC_000023.11:9089556:A:AAA,NC_000023.11:9089556:A:AAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
AA=0.00819/91 (TOMMO)
HGVS:: NC_000023.11:g.9089557_9089558insAA, NC_000023.11:g.9089557_9089558insAAAA, NC_000023.10:g.9057598_9057599insAA, NC_000023.10:g.9057598_9057599insAAAA

Select item 149129434819.

rs1491294348 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA [Show Flanks]
Chromosome:: X:9142401 (GRCh38)
X:9110443 (GRCh37)
Canonical SPDI:: NC_000023.11:9142401::A,NC_000023.11:9142401::ATA,NC_000023.11:9142401::ATATA,NC_000023.11:9142401::ATATATA,NC_000023.11:9142401::ATATATATA,NC_000023.11:9142401::ATATATATATA,NC_000023.11:9142401::ATATATATATATA,NC_000023.11:9142401::ATATATATATATATA
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000023.11:g.9142401_9142402insA, NC_000023.11:g.9142401_9142402insATA, NC_000023.11:g.9142401_9142402insATATA, NC_000023.11:g.9142401_9142402insATATATA, NC_000023.11:g.9142401_9142402insATATATATA, NC_000023.11:g.9142401_9142402insATATATATATA, NC_000023.11:g.9142401_9142402insATATATATATATA, NC_000023.11:g.9142401_9142402insATATATATATATATA, NC_000023.10:g.9110442_9110443insA, NC_000023.10:g.9110442_9110443insATA, NC_000023.10:g.9110442_9110443insATATA, NC_000023.10:g.9110442_9110443insATATATA, NC_000023.10:g.9110442_9110443insATATATATA, NC_000023.10:g.9110442_9110443insATATATATATA, NC_000023.10:g.9110442_9110443insATATATATATATA, NC_000023.10:g.9110442_9110443insATATATATATATATA

Select item 149128550520.

rs1491285505 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: X:9104193 (GRCh38)
X:9072235 (GRCh37)
Canonical SPDI:: NC_000023.11:9104193::C
Validated:: by frequency,by alfa
MAF:: C=0.00017/2 (ALFA)
HGVS:: NC_000023.11:g.9104193_9104194insC, NC_000023.10:g.9072234_9072235insC

<< First< Prev

Page of 50

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1000

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity