SNP Links for Gene (Select 5241) - SNP

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Select item 14915853401.

rs1491585340 has merged into rs112288755 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 11:101093325 (GRCh38)
11:100964056 (GRCh37)
Canonical SPDI:: NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:101093312:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.1/4 (GENOME_DK)
T=0.125/75 (NorthernSweden)
T=0.14497/726 (1000Genomes)
HGVS:: NC_000011.10:g.101093325_101093326del, NC_000011.10:g.101093326del, NC_000011.10:g.101093326dup, NC_000011.10:g.101093325_101093326dup, NC_000011.10:g.101093324_101093326dup, NC_000011.10:g.101093323_101093326dup, NC_000011.9:g.100964056_100964057del, NC_000011.9:g.100964057del, NC_000011.9:g.100964057dup, NC_000011.9:g.100964056_100964057dup, NC_000011.9:g.100964055_100964057dup, NC_000011.9:g.100964054_100964057dup, NG_016475.1:g.41500_41501del, NG_016475.1:g.41501del, NG_016475.1:g.41501dup, NG_016475.1:g.41500_41501dup, NG_016475.1:g.41499_41501dup, NG_016475.1:g.41498_41501dup

Select item 14915780762.

rs1491578076 has merged into rs57854947 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,AAA,AAAA,AAAAAA [Show Flanks]
Chromosome:: 11:101085372 (GRCh38)
11:100956103 (GRCh37)
Canonical SPDI:: NC_000011.10:101085367:AAAAAAAAA:AAAA,NC_000011.10:101085367:AAAAAAAAA:AAAAAAA,NC_000011.10:101085367:AAAAAAAAA:AAAAAAAA,NC_000011.10:101085367:AAAAAAAAA:AAAAAAAAAA
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAA=0./0 (ALFA)
-=0.000259/1 (ALSPAC)
A=0.331663/331 (GoNL)
A=0.405/243 (NorthernSweden)
A=0.411995/109051 (TOPMED)
-=0.458569/2269 (1000Genomes)
A=0.5/20 (GENOME_DK)
HGVS:: NC_000011.10:g.101085372_101085376del, NC_000011.10:g.101085375_101085376del, NC_000011.10:g.101085376del, NC_000011.10:g.101085376dup, NC_000011.9:g.100956103_100956107del, NC_000011.9:g.100956106_100956107del, NC_000011.9:g.100956107del, NC_000011.9:g.100956107dup, NG_016475.1:g.49442_49446del, NG_016475.1:g.49445_49446del, NG_016475.1:g.49446del, NG_016475.1:g.49446dup

Select item 14915554823.

rs1491555482 has merged into rs377349747 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:101105507 (GRCh38)
11:100976238 (GRCh37)
Canonical SPDI:: NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101105495:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.165/636 (ALSPAC)
-=0.4008/2007 (1000Genomes)
HGVS:: NC_000011.10:g.101105507_101105513del, NC_000011.10:g.101105510_101105513del, NC_000011.10:g.101105511_101105513del, NC_000011.10:g.101105512_101105513del, NC_000011.10:g.101105513del, NC_000011.10:g.101105513dup, NC_000011.10:g.101105512_101105513dup, NC_000011.10:g.101105511_101105513dup, NC_000011.10:g.101105510_101105513dup, NC_000011.10:g.101105500_101105513dup, NC_000011.9:g.100976238_100976244del, NC_000011.9:g.100976241_100976244del, NC_000011.9:g.100976242_100976244del, NC_000011.9:g.100976243_100976244del, NC_000011.9:g.100976244del, NC_000011.9:g.100976244dup, NC_000011.9:g.100976243_100976244dup, NC_000011.9:g.100976242_100976244dup, NC_000011.9:g.100976241_100976244dup, NC_000011.9:g.100976231_100976244dup, NG_016475.1:g.29312_29318del, NG_016475.1:g.29315_29318del, NG_016475.1:g.29316_29318del, NG_016475.1:g.29317_29318del, NG_016475.1:g.29318del, NG_016475.1:g.29318dup, NG_016475.1:g.29317_29318dup, NG_016475.1:g.29316_29318dup, NG_016475.1:g.29315_29318dup, NG_016475.1:g.29305_29318dup

Select item 14913963384.

rs1491396338 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:101116739 (GRCh38)
11:100987470 (GRCh37)
Canonical SPDI:: NC_000011.10:101116738:CA:
Gene:: PGR (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000011.10:g.101116739_101116740del, NC_000011.9:g.100987470_100987471del, NG_016475.1:g.18074_18075del, XM_011542869.3:c.*3532_*3533del, XM_011542869.2:c.*3532_*3533del

Select item 14913841435.

rs1491384143 has merged into rs59106149 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:101076932 (GRCh38)
11:100947663 (GRCh37)
Canonical SPDI:: NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:101076919:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTT=0.4756/2382 (1000Genomes)
HGVS:: NC_000011.10:g.101076932_101076945del, NC_000011.10:g.101076933_101076945del, NC_000011.10:g.101076934_101076945del, NC_000011.10:g.101076935_101076945del, NC_000011.10:g.101076936_101076945del, NC_000011.10:g.101076937_101076945del, NC_000011.10:g.101076938_101076945del, NC_000011.10:g.101076939_101076945del, NC_000011.10:g.101076940_101076945del, NC_000011.10:g.101076941_101076945del, NC_000011.10:g.101076942_101076945del, NC_000011.10:g.101076943_101076945del, NC_000011.10:g.101076944_101076945del, NC_000011.10:g.101076945del, NC_000011.10:g.101076945dup, NC_000011.10:g.101076944_101076945dup, NC_000011.10:g.101076943_101076945dup, NC_000011.10:g.101076942_101076945dup, NC_000011.10:g.101076941_101076945dup, NC_000011.10:g.101076940_101076945dup, NC_000011.10:g.101076939_101076945dup, NC_000011.10:g.101076938_101076945dup, NC_000011.10:g.101076937_101076945dup, NC_000011.10:g.101076936_101076945dup, NC_000011.10:g.101076935_101076945dup, NC_000011.10:g.101076934_101076945dup, NC_000011.10:g.101076933_101076945dup, NC_000011.10:g.101076932_101076945dup, NC_000011.10:g.101076930_101076945dup, NC_000011.10:g.101076929_101076945dup, NC_000011.9:g.100947663_100947676del, NC_000011.9:g.100947664_100947676del, NC_000011.9:g.100947665_100947676del, NC_000011.9:g.100947666_100947676del, NC_000011.9:g.100947667_100947676del, NC_000011.9:g.100947668_100947676del, NC_000011.9:g.100947669_100947676del, NC_000011.9:g.100947670_100947676del, NC_000011.9:g.100947671_100947676del, NC_000011.9:g.100947672_100947676del, NC_000011.9:g.100947673_100947676del, NC_000011.9:g.100947674_100947676del, NC_000011.9:g.100947675_100947676del, NC_000011.9:g.100947676del, NC_000011.9:g.100947676dup, NC_000011.9:g.100947675_100947676dup, NC_000011.9:g.100947674_100947676dup, NC_000011.9:g.100947673_100947676dup, NC_000011.9:g.100947672_100947676dup, NC_000011.9:g.100947671_100947676dup, NC_000011.9:g.100947670_100947676dup, NC_000011.9:g.100947669_100947676dup, NC_000011.9:g.100947668_100947676dup, NC_000011.9:g.100947667_100947676dup, NC_000011.9:g.100947666_100947676dup, NC_000011.9:g.100947665_100947676dup, NC_000011.9:g.100947664_100947676dup, NC_000011.9:g.100947663_100947676dup, NC_000011.9:g.100947661_100947676dup, NC_000011.9:g.100947660_100947676dup, NG_016475.1:g.57881_57894del, NG_016475.1:g.57882_57894del, NG_016475.1:g.57883_57894del, NG_016475.1:g.57884_57894del, NG_016475.1:g.57885_57894del, NG_016475.1:g.57886_57894del, NG_016475.1:g.57887_57894del, NG_016475.1:g.57888_57894del, NG_016475.1:g.57889_57894del, NG_016475.1:g.57890_57894del, NG_016475.1:g.57891_57894del, NG_016475.1:g.57892_57894del, NG_016475.1:g.57893_57894del, NG_016475.1:g.57894del, NG_016475.1:g.57894dup, NG_016475.1:g.57893_57894dup, NG_016475.1:g.57892_57894dup, NG_016475.1:g.57891_57894dup, NG_016475.1:g.57890_57894dup, NG_016475.1:g.57889_57894dup, NG_016475.1:g.57888_57894dup, NG_016475.1:g.57887_57894dup, NG_016475.1:g.57886_57894dup, NG_016475.1:g.57885_57894dup, NG_016475.1:g.57884_57894dup, NG_016475.1:g.57883_57894dup, NG_016475.1:g.57882_57894dup, NG_016475.1:g.57881_57894dup, NG_016475.1:g.57879_57894dup, NG_016475.1:g.57878_57894dup

Select item 14912113256.

rs1491211325 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:101076919 (GRCh38)
11:100947650 (GRCh37)
Canonical SPDI:: NC_000011.10:101076918:AT:
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00014/2 (TOMMO)
HGVS:: NC_000011.10:g.101076919_101076920del, NC_000011.9:g.100947650_100947651del, NG_016475.1:g.57894_57895del

Select item 14911974167.

rs1491197416 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:101059842 (GRCh38)
11:100930573 (GRCh37)
Canonical SPDI:: NC_000011.10:101059841:CA:
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00043/11 (TOMMO)
HGVS:: NC_000011.10:g.101059842_101059843del, NC_000011.9:g.100930573_100930574del, NG_016475.1:g.74971_74972del

Select item 14911888378.

rs1491188837 has merged into rs11300466 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:101116750 (GRCh38)
11:100987481 (GRCh37)
Canonical SPDI:: NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101116739:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000011.10:g.101116750_101116762del, NC_000011.10:g.101116758_101116762del, NC_000011.10:g.101116760_101116762del, NC_000011.10:g.101116761_101116762del, NC_000011.10:g.101116762del, NC_000011.10:g.101116762dup, NC_000011.10:g.101116761_101116762dup, NC_000011.10:g.101116760_101116762dup, NC_000011.10:g.101116759_101116762dup, NC_000011.10:g.101116758_101116762dup, NC_000011.10:g.101116757_101116762dup, NC_000011.10:g.101116756_101116762dup, NC_000011.10:g.101116752_101116762dup, NC_000011.10:g.101116751_101116762dup, NC_000011.10:g.101116745_101116762dup, NC_000011.10:g.101116742_101116762dup, NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101116762_101116763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100987481_100987493del, NC_000011.9:g.100987489_100987493del, NC_000011.9:g.100987491_100987493del, NC_000011.9:g.100987492_100987493del, NC_000011.9:g.100987493del, NC_000011.9:g.100987493dup, NC_000011.9:g.100987492_100987493dup, NC_000011.9:g.100987491_100987493dup, NC_000011.9:g.100987490_100987493dup, NC_000011.9:g.100987489_100987493dup, NC_000011.9:g.100987488_100987493dup, NC_000011.9:g.100987487_100987493dup, NC_000011.9:g.100987483_100987493dup, NC_000011.9:g.100987482_100987493dup, NC_000011.9:g.100987476_100987493dup, NC_000011.9:g.100987473_100987493dup, NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100987493_100987494insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016475.1:g.18062_18074del, NG_016475.1:g.18070_18074del, NG_016475.1:g.18072_18074del, NG_016475.1:g.18073_18074del, NG_016475.1:g.18074del, NG_016475.1:g.18074dup, NG_016475.1:g.18073_18074dup, NG_016475.1:g.18072_18074dup, NG_016475.1:g.18071_18074dup, NG_016475.1:g.18070_18074dup, NG_016475.1:g.18069_18074dup, NG_016475.1:g.18068_18074dup, NG_016475.1:g.18064_18074dup, NG_016475.1:g.18063_18074dup, NG_016475.1:g.18057_18074dup, NG_016475.1:g.18054_18074dup, NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.18074_18075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011542869.3:c.*3520_*3532del, XM_011542869.3:c.*3528_*3532del, XM_011542869.3:c.*3530_*3532del, XM_011542869.3:c.*3531_*3532del, XM_011542869.3:c.*3532del, XM_011542869.3:c.*3532dup, XM_011542869.3:c.*3531_*3532dup, XM_011542869.3:c.*3530_*3532dup, XM_011542869.3:c.*3529_*3532dup, XM_011542869.3:c.*3528_*3532dup, XM_011542869.3:c.*3527_*3532dup, XM_011542869.3:c.*3526_*3532dup, XM_011542869.3:c.*3522_*3532dup, XM_011542869.3:c.*3521_*3532dup, XM_011542869.3:c.*3515_*3532dup, XM_011542869.3:c.*3512_*3532dup, XM_011542869.3:c.*3532_*3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011542869.3:c.*3532_*3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011542869.2:c.*3520_*3532del, XM_011542869.2:c.*3528_*3532del, XM_011542869.2:c.*3530_*3532del, XM_011542869.2:c.*3531_*3532del, XM_011542869.2:c.*3532del, XM_011542869.2:c.*3532dup, XM_011542869.2:c.*3531_*3532dup, XM_011542869.2:c.*3530_*3532dup, XM_011542869.2:c.*3529_*3532dup, XM_011542869.2:c.*3528_*3532dup, XM_011542869.2:c.*3527_*3532dup, XM_011542869.2:c.*3526_*3532dup, XM_011542869.2:c.*3522_*3532dup, XM_011542869.2:c.*3521_*3532dup, XM_011542869.2:c.*3515_*3532dup, XM_011542869.2:c.*3512_*3532dup, XM_011542869.2:c.*3532_*3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011542869.2:c.*3532_*3533insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14911800959.

rs1491180095 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 11:101093313 (GRCh38)
11:100964045 (GRCh37)
Canonical SPDI:: NC_000011.10:101093313::G
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.101093313_101093314insG, NC_000011.9:g.100964044_100964045insG, NG_016475.1:g.41500_41501insC

Select item 149107136610.

rs1491071366 has merged into rs141102184 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA [Show Flanks]
Chromosome:: 11:101079431 (GRCh38)
11:100950162 (GRCh37)
Canonical SPDI:: NC_000011.10:101079421:AAAAAAAAAAA:AAAAAAAAA,NC_000011.10:101079421:AAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:101079421:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:101079421:AAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:101079421:AAAAAAAAAAA:AAAAAAAAAAAAAA
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.17123/588 (1000Genomes)
HGVS:: NC_000011.10:g.101079431_101079432del, NC_000011.10:g.101079432del, NC_000011.10:g.101079432dup, NC_000011.10:g.101079431_101079432dup, NC_000011.10:g.101079430_101079432dup, NC_000011.9:g.100950162_100950163del, NC_000011.9:g.100950163del, NC_000011.9:g.100950163dup, NC_000011.9:g.100950162_100950163dup, NC_000011.9:g.100950161_100950163dup, NG_016475.1:g.55391_55392del, NG_016475.1:g.55392del, NG_016475.1:g.55392dup, NG_016475.1:g.55391_55392dup, NG_016475.1:g.55390_55392dup

Select item 149106577311.

rs1491065773 has merged into rs113646711 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA [Show Flanks]
Chromosome:: 11:101084668 (GRCh38)
11:100955399 (GRCh37)
Canonical SPDI:: NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:101084656:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.41511/1868 (1000Genomes)
HGVS:: NC_000011.10:g.101084668_101084670del, NC_000011.10:g.101084669_101084670del, NC_000011.10:g.101084670del, NC_000011.10:g.101084670dup, NC_000011.10:g.101084669_101084670dup, NC_000011.10:g.101084668_101084670dup, NC_000011.9:g.100955399_100955401del, NC_000011.9:g.100955400_100955401del, NC_000011.9:g.100955401del, NC_000011.9:g.100955401dup, NC_000011.9:g.100955400_100955401dup, NC_000011.9:g.100955399_100955401dup, NG_016475.1:g.50155_50157del, NG_016475.1:g.50156_50157del, NG_016475.1:g.50157del, NG_016475.1:g.50157dup, NG_016475.1:g.50156_50157dup, NG_016475.1:g.50155_50157dup

Select item 149105845812.

rs1491058458 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 11:101069544 (GRCh38)
11:100940276 (GRCh37)
Canonical SPDI:: NC_000011.10:101069544:AA:AAA
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AAA=0./0 (ALFA)
HGVS:: NC_000011.10:g.101069546dup, NC_000011.9:g.100940277dup, NG_016475.1:g.65269dup

Select item 149103730113.

rs1491037301 has merged into rs1277666246 [Homo sapiens]

Variant type:: DELINS
Alleles:: CGTGTGTGTGTG>-,CGTGTGTGTGTGCGTGTGTGTGTG [Show Flanks]
Chromosome:: 11:101060192 (GRCh38)
11:100930923 (GRCh37)
Canonical SPDI:: NC_000011.10:101060180:GTGTGTGTGTGCGTGTGTGTGTG:GTGTGTGTGTG,NC_000011.10:101060180:GTGTGTGTGTGCGTGTGTGTGTG:GTGTGTGTGTGCGTGTGTGTGTGCGTGTGTGTGTG
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTG=0.000108/2 (ALFA)
GTGTGTGTGTGC=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.101060192_101060203del, NC_000011.10:g.101060192_101060203dup, NC_000011.9:g.100930923_100930934del, NC_000011.9:g.100930923_100930934dup, NG_016475.1:g.74622_74633del, NG_016475.1:g.74622_74633dup

Select item 149102080614.

rs1491020806 has merged into rs3067562 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCTCT>-,CT,CTCT,CTCTCT,CTCTCTCTCT,CTCTCTCTCTCT,CTCTCTCTCTCTCTCT [Show Flanks]
Chromosome:: 11:101082136 (GRCh38)
11:100952867 (GRCh37)
Canonical SPDI:: NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT,NC_000011.10:101082125:CTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCT
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCTCTCTCTCT=0./0 (ALFA)
CT=0.10333/62 (NorthernSweden)
CT=0.125/5 (GENOME_DK)
HGVS:: NC_000011.10:g.101082126CT[5], NC_000011.10:g.101082126CT[6], NC_000011.10:g.101082126CT[7], NC_000011.10:g.101082126CT[8], NC_000011.10:g.101082126CT[10], NC_000011.10:g.101082126CT[11], NC_000011.10:g.101082126CT[13], NC_000011.9:g.100952857CT[5], NC_000011.9:g.100952857CT[6], NC_000011.9:g.100952857CT[7], NC_000011.9:g.100952857CT[8], NC_000011.9:g.100952857CT[10], NC_000011.9:g.100952857CT[11], NC_000011.9:g.100952857CT[13], NG_016475.1:g.52671AG[5], NG_016475.1:g.52671AG[6], NG_016475.1:g.52671AG[7], NG_016475.1:g.52671AG[8], NG_016475.1:g.52671AG[10], NG_016475.1:g.52671AG[11], NG_016475.1:g.52671AG[13]

Select item 149101370715.

rs1491013707 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT [Show Flanks]
Chromosome:: 11:101045697 (GRCh38)
11:100916428 (GRCh37)
Canonical SPDI:: NC_000011.10:101045695:TAT:T,NC_000011.10:101045695:TAT:TATAT
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
-=0.00028/5 (TOMMO)
HGVS:: NC_000011.10:g.101045697_101045698del, NC_000011.10:g.101045697_101045698dup, NC_000011.9:g.100916428_100916429del, NC_000011.9:g.100916428_100916429dup, NG_016475.1:g.89117_89118del, NG_016475.1:g.89117_89118dup

Select item 149100467016.

rs1491004670 has merged into rs56355097 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:101107878 (GRCh38)
11:100978609 (GRCh37)
Canonical SPDI:: NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:101107865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PGR (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.265/1327 (1000Genomes)
HGVS:: NC_000011.10:g.101107878_101107880del, NC_000011.10:g.101107879_101107880del, NC_000011.10:g.101107880del, NC_000011.10:g.101107880dup, NC_000011.10:g.101107879_101107880dup, NC_000011.10:g.101107878_101107880dup, NC_000011.10:g.101107877_101107880dup, NC_000011.10:g.101107876_101107880dup, NC_000011.10:g.101107875_101107880dup, NC_000011.10:g.101107874_101107880dup, NC_000011.10:g.101107873_101107880dup, NC_000011.10:g.101107872_101107880dup, NC_000011.10:g.101107871_101107880dup, NC_000011.10:g.101107870_101107880dup, NC_000011.10:g.101107869_101107880dup, NC_000011.10:g.101107868_101107880dup, NC_000011.10:g.101107867_101107880dup, NC_000011.10:g.101107866_101107880dup, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107880_101107881insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.101107866_101107880A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000011.9:g.100978609_100978611del, NC_000011.9:g.100978610_100978611del, NC_000011.9:g.100978611del, NC_000011.9:g.100978611dup, NC_000011.9:g.100978610_100978611dup, NC_000011.9:g.100978609_100978611dup, NC_000011.9:g.100978608_100978611dup, NC_000011.9:g.100978607_100978611dup, NC_000011.9:g.100978606_100978611dup, NC_000011.9:g.100978605_100978611dup, NC_000011.9:g.100978604_100978611dup, NC_000011.9:g.100978603_100978611dup, NC_000011.9:g.100978602_100978611dup, NC_000011.9:g.100978601_100978611dup, NC_000011.9:g.100978600_100978611dup, NC_000011.9:g.100978599_100978611dup, NC_000011.9:g.100978598_100978611dup, NC_000011.9:g.100978597_100978611dup, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978611_100978612insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.100978597_100978611A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016475.1:g.26946_26948del, NG_016475.1:g.26947_26948del, NG_016475.1:g.26948del, NG_016475.1:g.26948dup, NG_016475.1:g.26947_26948dup, NG_016475.1:g.26946_26948dup, NG_016475.1:g.26945_26948dup, NG_016475.1:g.26944_26948dup, NG_016475.1:g.26943_26948dup, NG_016475.1:g.26942_26948dup, NG_016475.1:g.26941_26948dup, NG_016475.1:g.26940_26948dup, NG_016475.1:g.26939_26948dup, NG_016475.1:g.26938_26948dup, NG_016475.1:g.26937_26948dup, NG_016475.1:g.26936_26948dup, NG_016475.1:g.26935_26948dup, NG_016475.1:g.26934_26948dup, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26948_26949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016475.1:g.26934_26948T[55]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149099110617.

rs1490991106 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:101100368 (GRCh38)
11:100971099 (GRCh37)
Canonical SPDI:: NC_000011.10:101100367:C:T
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.101100368C>T, NC_000011.9:g.100971099C>T, NG_016475.1:g.34446G>A

Select item 149098195518.

rs1490981955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:101115458 (GRCh38)
11:100986189 (GRCh37)
Canonical SPDI:: NC_000011.10:101115457:G:T
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,downstream_transcript_variant,intron_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.101115458G>T, NC_000011.9:g.100986189G>T, NG_016475.1:g.19356C>A

Select item 149092789019.

rs1490927890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:101131222 (GRCh38)
11:101001953 (GRCh37)
Canonical SPDI:: NC_000011.10:101131221:A:G
Gene:: PGR (Varview), PGR-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.101131222A>G, NC_000011.9:g.101001953A>G, NG_016475.1:g.3592T>C

Select item 149085226620.

rs1490852266 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:101088466 (GRCh38)
11:100959197 (GRCh37)
Canonical SPDI:: NC_000011.10:101088465:G:A
Gene:: PGR (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.101088466G>A, NC_000011.9:g.100959197G>A, NG_016475.1:g.46348C>T

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