SNP Links for Gene (Select 55811) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915683121.

rs1491568312 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 1:167851177 (GRCh38)
1:167820415 (GRCh37)
Canonical SPDI:: NC_000001.11:167851174:TTTT:TT
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0.000285/4 (ALFA)
-=0.000484/128 (TOPMED)
-=0.000493/69 (GnomAD)
HGVS:: NC_000001.11:g.167851177_167851178del, NC_000001.10:g.167820415_167820416del, NG_016139.2:g.67958_67959del, NG_016139.1:g.68040_68041del

Select item 14915591952.

rs1491559195 has merged into rs67534872 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:167898605 (GRCh38)
1:167867843 (GRCh37)
Canonical SPDI:: NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:167898594:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0./0 (ALSPAC)
T=0./0 (TWINSUK)
T=0.0182/91 (1000Genomes)
HGVS:: NC_000001.11:g.167898605_167898607del, NC_000001.11:g.167898606_167898607del, NC_000001.11:g.167898607del, NC_000001.11:g.167898607dup, NC_000001.11:g.167898606_167898607dup, NC_000001.11:g.167898596_167898607dup, NC_000001.10:g.167867843_167867845del, NC_000001.10:g.167867844_167867845del, NC_000001.10:g.167867845del, NC_000001.10:g.167867845dup, NC_000001.10:g.167867844_167867845dup, NC_000001.10:g.167867834_167867845dup, NG_016139.2:g.20537_20539del, NG_016139.2:g.20538_20539del, NG_016139.2:g.20539del, NG_016139.2:g.20539dup, NG_016139.2:g.20538_20539dup, NG_016139.2:g.20528_20539dup, NG_016139.1:g.20619_20621del, NG_016139.1:g.20620_20621del, NG_016139.1:g.20621del, NG_016139.1:g.20621dup, NG_016139.1:g.20620_20621dup, NG_016139.1:g.20610_20621dup

Select item 14915348723.

rs1491534872 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:167893695 (GRCh38)
1:167862933 (GRCh37)
Canonical SPDI:: NC_000001.11:167893694:CA:
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.0032/38 (ALFA)
HGVS:: NC_000001.11:g.167893695_167893696del, NC_000001.10:g.167862933_167862934del, NG_016139.2:g.25438_25439del, NG_016139.1:g.25520_25521del

Select item 14914719344.

rs1491471934 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:167853856 (GRCh38)
1:167823094 (GRCh37)
Canonical SPDI:: NC_000001.11:167853855:TG:
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.167853856_167853857del, NC_000001.10:g.167823094_167823095del, NG_016139.2:g.65277_65278del, NG_016139.1:g.65359_65360del

Select item 14914669965.

rs1491466996 has merged into rs748872658 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:167893704 (GRCh38)
1:167862942 (GRCh37)
Canonical SPDI:: NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167893695:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Clinical significance:: benign,likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.167893704_167893719del, NC_000001.11:g.167893705_167893719del, NC_000001.11:g.167893706_167893719del, NC_000001.11:g.167893708_167893719del, NC_000001.11:g.167893709_167893719del, NC_000001.11:g.167893710_167893719del, NC_000001.11:g.167893712_167893719del, NC_000001.11:g.167893713_167893719del, NC_000001.11:g.167893714_167893719del, NC_000001.11:g.167893715_167893719del, NC_000001.11:g.167893716_167893719del, NC_000001.11:g.167893717_167893719del, NC_000001.11:g.167893718_167893719del, NC_000001.11:g.167893719del, NC_000001.11:g.167893719dup, NC_000001.11:g.167893718_167893719dup, NC_000001.11:g.167893717_167893719dup, NC_000001.11:g.167893715_167893719dup, NC_000001.11:g.167893714_167893719dup, NC_000001.11:g.167893713_167893719dup, NC_000001.11:g.167893705_167893719dup, NC_000001.10:g.167862942_167862957del, NC_000001.10:g.167862943_167862957del, NC_000001.10:g.167862944_167862957del, NC_000001.10:g.167862946_167862957del, NC_000001.10:g.167862947_167862957del, NC_000001.10:g.167862948_167862957del, NC_000001.10:g.167862950_167862957del, NC_000001.10:g.167862951_167862957del, NC_000001.10:g.167862952_167862957del, NC_000001.10:g.167862953_167862957del, NC_000001.10:g.167862954_167862957del, NC_000001.10:g.167862955_167862957del, NC_000001.10:g.167862956_167862957del, NC_000001.10:g.167862957del, NC_000001.10:g.167862957dup, NC_000001.10:g.167862956_167862957dup, NC_000001.10:g.167862955_167862957dup, NC_000001.10:g.167862953_167862957dup, NC_000001.10:g.167862952_167862957dup, NC_000001.10:g.167862951_167862957dup, NC_000001.10:g.167862943_167862957dup, NG_016139.2:g.25423_25438del, NG_016139.2:g.25424_25438del, NG_016139.2:g.25425_25438del, NG_016139.2:g.25427_25438del, NG_016139.2:g.25428_25438del, NG_016139.2:g.25429_25438del, NG_016139.2:g.25431_25438del, NG_016139.2:g.25432_25438del, NG_016139.2:g.25433_25438del, NG_016139.2:g.25434_25438del, NG_016139.2:g.25435_25438del, NG_016139.2:g.25436_25438del, NG_016139.2:g.25437_25438del, NG_016139.2:g.25438del, NG_016139.2:g.25438dup, NG_016139.2:g.25437_25438dup, NG_016139.2:g.25436_25438dup, NG_016139.2:g.25434_25438dup, NG_016139.2:g.25433_25438dup, NG_016139.2:g.25432_25438dup, NG_016139.2:g.25424_25438dup, NG_016139.1:g.25505_25520del, NG_016139.1:g.25506_25520del, NG_016139.1:g.25507_25520del, NG_016139.1:g.25509_25520del, NG_016139.1:g.25510_25520del, NG_016139.1:g.25511_25520del, NG_016139.1:g.25513_25520del, NG_016139.1:g.25514_25520del, NG_016139.1:g.25515_25520del, NG_016139.1:g.25516_25520del, NG_016139.1:g.25517_25520del, NG_016139.1:g.25518_25520del, NG_016139.1:g.25519_25520del, NG_016139.1:g.25520del, NG_016139.1:g.25520dup, NG_016139.1:g.25519_25520dup, NG_016139.1:g.25518_25520dup, NG_016139.1:g.25516_25520dup, NG_016139.1:g.25515_25520dup, NG_016139.1:g.25514_25520dup, NG_016139.1:g.25506_25520dup

Select item 14914595796.

rs1491459579 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:167825322 (GRCh38)
1:167794560 (GRCh37)
Canonical SPDI:: NC_000001.11:167825321:CT:
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.167825322_167825323del, NC_000001.10:g.167794560_167794561del, NG_016139.2:g.93811_93812del, NG_016139.1:g.93893_93894del

Select item 14914035877.

rs1491403587 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:167898594 (GRCh38)
1:167867832 (GRCh37)
Canonical SPDI:: NC_000001.11:167898593:GT:
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00003/1 (GnomAD)
HGVS:: NC_000001.11:g.167898594_167898595del, NC_000001.10:g.167867832_167867833del, NG_016139.2:g.20539_20540del, NG_016139.1:g.20621_20622del

Select item 14914016748.

rs1491401674 has merged into rs10599580 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA [Show Flanks]
Chromosome:: 1:167827717 (GRCh38)
1:167796955 (GRCh37)
Canonical SPDI:: NC_000001.11:167827707:AAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:167827707:AAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:167827707:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:167827707:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:167827707:AAAAAAAAAAAA:AAAAAAAAAAAAAA
Gene:: ADCY10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.3262/593 (Korea1K)
-=0.4964/2486 (1000Genomes)
HGVS:: NC_000001.11:g.167827717_167827719del, NC_000001.11:g.167827718_167827719del, NC_000001.11:g.167827719del, NC_000001.11:g.167827719dup, NC_000001.11:g.167827718_167827719dup, NC_000001.10:g.167796955_167796957del, NC_000001.10:g.167796956_167796957del, NC_000001.10:g.167796957del, NC_000001.10:g.167796957dup, NC_000001.10:g.167796956_167796957dup, NG_016139.2:g.91424_91426del, NG_016139.2:g.91425_91426del, NG_016139.2:g.91426del, NG_016139.2:g.91426dup, NG_016139.2:g.91425_91426dup, NG_016139.1:g.91506_91508del, NG_016139.1:g.91507_91508del, NG_016139.1:g.91508del, NG_016139.1:g.91508dup, NG_016139.1:g.91507_91508dup

Select item 14913499909.

rs1491349990 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:167875432 (GRCh38)
1:167844670 (GRCh37)
Canonical SPDI:: NC_000001.11:167875430:TGT:T
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.0337/125 (TWINSUK)
-=0.0343/132 (ALSPAC)
HGVS:: NC_000001.11:g.167875432_167875433del, NC_000001.10:g.167844670_167844671del, NG_016139.2:g.43702_43703del, NG_016139.1:g.43784_43785del

Select item 149132312910.

rs1491323129 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:167858497 (GRCh38)
1:167827735 (GRCh37)
Canonical SPDI:: NC_000001.11:167858496:CA:
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00042/5 (ALFA)
-=0.00277/77 (TOMMO)
HGVS:: NC_000001.11:g.167858497_167858498del, NC_000001.10:g.167827735_167827736del, NG_016139.2:g.60636_60637del, NG_016139.1:g.60718_60719del

Select item 149131801311.

rs1491318013 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 1:167884694 (GRCh38)
1:167853932 (GRCh37)
Canonical SPDI:: NC_000001.11:167884693:AT:
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.000084/1 (ALFA)
-=0.000101/11 (GnomAD)
HGVS:: NC_000001.11:g.167884694_167884695del, NC_000001.10:g.167853932_167853933del, NG_016139.2:g.34439_34440del, NG_016139.1:g.34521_34522del

Select item 149124741112.

rs1491247411 has merged into rs907113114 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT [Show Flanks]
Chromosome:: 1:167827728 (GRCh38)
1:167796966 (GRCh37)
Canonical SPDI:: NC_000001.11:167827719:TTTTTTTTTTT:TTTTTTTT,NC_000001.11:167827719:TTTTTTTTTTT:TTTTTTTTT,NC_000001.11:167827719:TTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:167827719:TTTTTTTTTTT:TTTTTTTTTTTT
Gene:: ADCY10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.001092/2 (Korea1K)
HGVS:: NC_000001.11:g.167827728_167827730del, NC_000001.11:g.167827729_167827730del, NC_000001.11:g.167827730del, NC_000001.11:g.167827730dup, NC_000001.10:g.167796966_167796968del, NC_000001.10:g.167796967_167796968del, NC_000001.10:g.167796968del, NC_000001.10:g.167796968dup, NG_016139.2:g.91412_91414del, NG_016139.2:g.91413_91414del, NG_016139.2:g.91414del, NG_016139.2:g.91414dup, NG_016139.1:g.91494_91496del, NG_016139.1:g.91495_91496del, NG_016139.1:g.91496del, NG_016139.1:g.91496dup

Select item 149117733113.

rs1491177331 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTA [Show Flanks]
Chromosome:: 1:167853856 (GRCh38)
1:167823095 (GRCh37)
Canonical SPDI:: NC_000001.11:167853856::TTA
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.167853856_167853857insTTA, NC_000001.10:g.167823094_167823095insTTA, NG_016139.2:g.65277_65278insTAA, NG_016139.1:g.65359_65360insTAA

Select item 149116297314.

rs1491162973 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 1:167827707 (GRCh38)
1:167796945 (GRCh37)
Canonical SPDI:: NC_000001.11:167827706:TA:
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00004/3 (GnomAD)
HGVS:: NC_000001.11:g.167827707_167827708del, NC_000001.10:g.167796945_167796946del, NG_016139.2:g.91426_91427del, NG_016139.1:g.91508_91509del

Select item 149116072915.

rs1491160729 [Homo sapiens]

Variant type:: DEL
Alleles:: CG>- [Show Flanks]
Chromosome:: 1:167850662 (GRCh38)
1:167819900 (GRCh37)
Canonical SPDI:: NC_000001.11:167850661:CG:
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.167850662_167850663del, NC_000001.10:g.167819900_167819901del, NG_016139.2:g.68471_68472del, NG_016139.1:g.68553_68554del

Select item 149113629816.

rs1491136298 has merged into rs57443879 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:167858507 (GRCh38)
1:167827745 (GRCh37)
Canonical SPDI:: NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167858497:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.167858507_167858522del, NC_000001.11:g.167858510_167858522del, NC_000001.11:g.167858511_167858522del, NC_000001.11:g.167858513_167858522del, NC_000001.11:g.167858514_167858522del, NC_000001.11:g.167858515_167858522del, NC_000001.11:g.167858516_167858522del, NC_000001.11:g.167858517_167858522del, NC_000001.11:g.167858518_167858522del, NC_000001.11:g.167858519_167858522del, NC_000001.11:g.167858520_167858522del, NC_000001.11:g.167858521_167858522del, NC_000001.11:g.167858522del, NC_000001.11:g.167858522dup, NC_000001.11:g.167858521_167858522dup, NC_000001.11:g.167858520_167858522dup, NC_000001.11:g.167858519_167858522dup, NC_000001.11:g.167858518_167858522dup, NC_000001.11:g.167858516_167858522dup, NC_000001.11:g.167858513_167858522dup, NC_000001.10:g.167827745_167827760del, NC_000001.10:g.167827748_167827760del, NC_000001.10:g.167827749_167827760del, NC_000001.10:g.167827751_167827760del, NC_000001.10:g.167827752_167827760del, NC_000001.10:g.167827753_167827760del, NC_000001.10:g.167827754_167827760del, NC_000001.10:g.167827755_167827760del, NC_000001.10:g.167827756_167827760del, NC_000001.10:g.167827757_167827760del, NC_000001.10:g.167827758_167827760del, NC_000001.10:g.167827759_167827760del, NC_000001.10:g.167827760del, NC_000001.10:g.167827760dup, NC_000001.10:g.167827759_167827760dup, NC_000001.10:g.167827758_167827760dup, NC_000001.10:g.167827757_167827760dup, NC_000001.10:g.167827756_167827760dup, NC_000001.10:g.167827754_167827760dup, NC_000001.10:g.167827751_167827760dup, NG_016139.2:g.60621_60636del, NG_016139.2:g.60624_60636del, NG_016139.2:g.60625_60636del, NG_016139.2:g.60627_60636del, NG_016139.2:g.60628_60636del, NG_016139.2:g.60629_60636del, NG_016139.2:g.60630_60636del, NG_016139.2:g.60631_60636del, NG_016139.2:g.60632_60636del, NG_016139.2:g.60633_60636del, NG_016139.2:g.60634_60636del, NG_016139.2:g.60635_60636del, NG_016139.2:g.60636del, NG_016139.2:g.60636dup, NG_016139.2:g.60635_60636dup, NG_016139.2:g.60634_60636dup, NG_016139.2:g.60633_60636dup, NG_016139.2:g.60632_60636dup, NG_016139.2:g.60630_60636dup, NG_016139.2:g.60627_60636dup, NG_016139.1:g.60703_60718del, NG_016139.1:g.60706_60718del, NG_016139.1:g.60707_60718del, NG_016139.1:g.60709_60718del, NG_016139.1:g.60710_60718del, NG_016139.1:g.60711_60718del, NG_016139.1:g.60712_60718del, NG_016139.1:g.60713_60718del, NG_016139.1:g.60714_60718del, NG_016139.1:g.60715_60718del, NG_016139.1:g.60716_60718del, NG_016139.1:g.60717_60718del, NG_016139.1:g.60718del, NG_016139.1:g.60718dup, NG_016139.1:g.60717_60718dup, NG_016139.1:g.60716_60718dup, NG_016139.1:g.60715_60718dup, NG_016139.1:g.60714_60718dup, NG_016139.1:g.60712_60718dup, NG_016139.1:g.60709_60718dup

Select item 149113101317.

rs1491131013 has merged into rs34844073 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:167825332 (GRCh38)
1:167794570 (GRCh37)
Canonical SPDI:: NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:167825322:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.3425/1715 (1000Genomes)
-=0.4585/1767 (ALSPAC)
-=0.4617/1712 (TWINSUK)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000001.11:g.167825332_167825337del, NC_000001.11:g.167825335_167825337del, NC_000001.11:g.167825336_167825337del, NC_000001.11:g.167825337del, NC_000001.11:g.167825337dup, NC_000001.11:g.167825336_167825337dup, NC_000001.11:g.167825335_167825337dup, NC_000001.11:g.167825325_167825337dup, NC_000001.10:g.167794570_167794575del, NC_000001.10:g.167794573_167794575del, NC_000001.10:g.167794574_167794575del, NC_000001.10:g.167794575del, NC_000001.10:g.167794575dup, NC_000001.10:g.167794574_167794575dup, NC_000001.10:g.167794573_167794575dup, NC_000001.10:g.167794563_167794575dup, NG_016139.2:g.93806_93811del, NG_016139.2:g.93809_93811del, NG_016139.2:g.93810_93811del, NG_016139.2:g.93811del, NG_016139.2:g.93811dup, NG_016139.2:g.93810_93811dup, NG_016139.2:g.93809_93811dup, NG_016139.2:g.93799_93811dup, NG_016139.1:g.93888_93893del, NG_016139.1:g.93891_93893del, NG_016139.1:g.93892_93893del, NG_016139.1:g.93893del, NG_016139.1:g.93893dup, NG_016139.1:g.93892_93893dup, NG_016139.1:g.93891_93893dup, NG_016139.1:g.93881_93893dup

Select item 149105370418.

rs1491053704 has merged into rs11306764 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAAA [Show Flanks]
Chromosome:: 1:167842601 (GRCh38)
1:167811839 (GRCh37)
Canonical SPDI:: NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAA,NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:167842591:AAAAAAAAAAA:AAAAAAAAAAAAAAAA
Gene:: ADCY10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
A=0.3954/1594 (1000Genomes)
HGVS:: NC_000001.11:g.167842601_167842602del, NC_000001.11:g.167842602del, NC_000001.11:g.167842602dup, NC_000001.11:g.167842601_167842602dup, NC_000001.11:g.167842600_167842602dup, NC_000001.11:g.167842598_167842602dup, NC_000001.10:g.167811839_167811840del, NC_000001.10:g.167811840del, NC_000001.10:g.167811840dup, NC_000001.10:g.167811839_167811840dup, NC_000001.10:g.167811838_167811840dup, NC_000001.10:g.167811836_167811840dup, NG_016139.2:g.76541_76542del, NG_016139.2:g.76542del, NG_016139.2:g.76542dup, NG_016139.2:g.76541_76542dup, NG_016139.2:g.76540_76542dup, NG_016139.2:g.76538_76542dup, NG_016139.1:g.76623_76624del, NG_016139.1:g.76624del, NG_016139.1:g.76624dup, NG_016139.1:g.76623_76624dup, NG_016139.1:g.76622_76624dup, NG_016139.1:g.76620_76624dup

Select item 149104551319.

rs1491045513 has merged into rs35237139 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA [Show Flanks]
Chromosome:: 1:167872378 (GRCh38)
1:167841616 (GRCh37)
Canonical SPDI:: NC_000001.11:167872367:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:167872367:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:167872367:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:167872367:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:167872367:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
A=0.2177/839 (ALSPAC)
A=0.2184/810 (TWINSUK)
-=0.2415/971 (1000Genomes)
HGVS:: NC_000001.11:g.167872378_167872380del, NC_000001.11:g.167872379_167872380del, NC_000001.11:g.167872380del, NC_000001.11:g.167872380dup, NC_000001.11:g.167872379_167872380dup, NC_000001.10:g.167841616_167841618del, NC_000001.10:g.167841617_167841618del, NC_000001.10:g.167841618del, NC_000001.10:g.167841618dup, NC_000001.10:g.167841617_167841618dup, NG_016139.2:g.46764_46766del, NG_016139.2:g.46765_46766del, NG_016139.2:g.46766del, NG_016139.2:g.46766dup, NG_016139.2:g.46765_46766dup, NG_016139.1:g.46846_46848del, NG_016139.1:g.46847_46848del, NG_016139.1:g.46848del, NG_016139.1:g.46848dup, NG_016139.1:g.46847_46848dup

Select item 149104158220.

rs1491041582 has merged into rs57450280 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:167866541 (GRCh38)
1:167835779 (GRCh37)
Canonical SPDI:: NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:167866530:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADCY10 (Varview), DCAF6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
AAAAAA=0.4469/2238 (1000Genomes)
HGVS:: NC_000001.11:g.167866541_167866551del, NC_000001.11:g.167866542_167866551del, NC_000001.11:g.167866543_167866551del, NC_000001.11:g.167866544_167866551del, NC_000001.11:g.167866545_167866551del, NC_000001.11:g.167866546_167866551del, NC_000001.11:g.167866547_167866551del, NC_000001.11:g.167866548_167866551del, NC_000001.11:g.167866549_167866551del, NC_000001.11:g.167866550_167866551del, NC_000001.11:g.167866551del, NC_000001.11:g.167866551dup, NC_000001.11:g.167866550_167866551dup, NC_000001.11:g.167866549_167866551dup, NC_000001.11:g.167866548_167866551dup, NC_000001.11:g.167866547_167866551dup, NC_000001.11:g.167866546_167866551dup, NC_000001.11:g.167866551_167866552insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.167835779_167835789del, NC_000001.10:g.167835780_167835789del, NC_000001.10:g.167835781_167835789del, NC_000001.10:g.167835782_167835789del, NC_000001.10:g.167835783_167835789del, NC_000001.10:g.167835784_167835789del, NC_000001.10:g.167835785_167835789del, NC_000001.10:g.167835786_167835789del, NC_000001.10:g.167835787_167835789del, NC_000001.10:g.167835788_167835789del, NC_000001.10:g.167835789del, NC_000001.10:g.167835789dup, NC_000001.10:g.167835788_167835789dup, NC_000001.10:g.167835787_167835789dup, NC_000001.10:g.167835786_167835789dup, NC_000001.10:g.167835785_167835789dup, NC_000001.10:g.167835784_167835789dup, NC_000001.10:g.167835789_167835790insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016139.2:g.52593_52603del, NG_016139.2:g.52594_52603del, NG_016139.2:g.52595_52603del, NG_016139.2:g.52596_52603del, NG_016139.2:g.52597_52603del, NG_016139.2:g.52598_52603del, NG_016139.2:g.52599_52603del, NG_016139.2:g.52600_52603del, NG_016139.2:g.52601_52603del, NG_016139.2:g.52602_52603del, NG_016139.2:g.52603del, NG_016139.2:g.52603dup, NG_016139.2:g.52602_52603dup, NG_016139.2:g.52601_52603dup, NG_016139.2:g.52600_52603dup, NG_016139.2:g.52599_52603dup, NG_016139.2:g.52598_52603dup, NG_016139.2:g.52603_52604insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016139.1:g.52675_52685del, NG_016139.1:g.52676_52685del, NG_016139.1:g.52677_52685del, NG_016139.1:g.52678_52685del, NG_016139.1:g.52679_52685del, NG_016139.1:g.52680_52685del, NG_016139.1:g.52681_52685del, NG_016139.1:g.52682_52685del, NG_016139.1:g.52683_52685del, NG_016139.1:g.52684_52685del, NG_016139.1:g.52685del, NG_016139.1:g.52685dup, NG_016139.1:g.52684_52685dup, NG_016139.1:g.52683_52685dup, NG_016139.1:g.52682_52685dup, NG_016139.1:g.52681_52685dup, NG_016139.1:g.52680_52685dup, NG_016139.1:g.52685_52686insTTTTTTTTTTTTTTTTTTTTTTTTTTT

<< First< Prev

Page of 50

Next >Last >>

dbSNP

Result Filters

Clinical Significance

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