SNP Links for Gene (Select 3568) - SNP

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Select item 14915849931.

rs1491584993 has merged into rs71058670 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:3070585 (GRCh38)
3:3112269 (GRCh37)
Canonical SPDI:: NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3070575:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.25/10 (GENOME_DK)
HGVS:: NC_000003.12:g.3070585_3070600del, NC_000003.12:g.3070586_3070600del, NC_000003.12:g.3070588_3070600del, NC_000003.12:g.3070589_3070600del, NC_000003.12:g.3070590_3070600del, NC_000003.12:g.3070591_3070600del, NC_000003.12:g.3070592_3070600del, NC_000003.12:g.3070593_3070600del, NC_000003.12:g.3070594_3070600del, NC_000003.12:g.3070595_3070600del, NC_000003.12:g.3070596_3070600del, NC_000003.12:g.3070597_3070600del, NC_000003.12:g.3070598_3070600del, NC_000003.12:g.3070599_3070600del, NC_000003.12:g.3070600del, NC_000003.12:g.3070600dup, NC_000003.12:g.3070599_3070600dup, NC_000003.12:g.3070598_3070600dup, NC_000003.12:g.3070597_3070600dup, NC_000003.12:g.3070596_3070600dup, NC_000003.12:g.3070595_3070600dup, NC_000003.12:g.3070594_3070600dup, NC_000003.12:g.3070593_3070600dup, NC_000003.12:g.3070592_3070600dup, NC_000003.12:g.3070591_3070600dup, NC_000003.12:g.3070590_3070600dup, NC_000003.12:g.3070589_3070600dup, NC_000003.12:g.3070588_3070600dup, NC_000003.12:g.3070587_3070600dup, NC_000003.12:g.3070586_3070600dup, NC_000003.12:g.3070585_3070600dup, NC_000003.12:g.3070584_3070600dup, NC_000003.12:g.3070583_3070600dup, NC_000003.12:g.3070582_3070600dup, NC_000003.12:g.3070581_3070600dup, NC_000003.12:g.3070580_3070600dup, NC_000003.12:g.3070579_3070600dup, NC_000003.12:g.3070578_3070600dup, NC_000003.12:g.3070577_3070600dup, NC_000003.11:g.3112269_3112284del, NC_000003.11:g.3112270_3112284del, NC_000003.11:g.3112272_3112284del, NC_000003.11:g.3112273_3112284del, NC_000003.11:g.3112274_3112284del, NC_000003.11:g.3112275_3112284del, NC_000003.11:g.3112276_3112284del, NC_000003.11:g.3112277_3112284del, NC_000003.11:g.3112278_3112284del, NC_000003.11:g.3112279_3112284del, NC_000003.11:g.3112280_3112284del, NC_000003.11:g.3112281_3112284del, NC_000003.11:g.3112282_3112284del, NC_000003.11:g.3112283_3112284del, NC_000003.11:g.3112284del, NC_000003.11:g.3112284dup, NC_000003.11:g.3112283_3112284dup, NC_000003.11:g.3112282_3112284dup, NC_000003.11:g.3112281_3112284dup, NC_000003.11:g.3112280_3112284dup, NC_000003.11:g.3112279_3112284dup, NC_000003.11:g.3112278_3112284dup, NC_000003.11:g.3112277_3112284dup, NC_000003.11:g.3112276_3112284dup, NC_000003.11:g.3112275_3112284dup, NC_000003.11:g.3112274_3112284dup, NC_000003.11:g.3112273_3112284dup, NC_000003.11:g.3112272_3112284dup, NC_000003.11:g.3112271_3112284dup, NC_000003.11:g.3112270_3112284dup, NC_000003.11:g.3112269_3112284dup, NC_000003.11:g.3112268_3112284dup, NC_000003.11:g.3112267_3112284dup, NC_000003.11:g.3112266_3112284dup, NC_000003.11:g.3112265_3112284dup, NC_000003.11:g.3112264_3112284dup, NC_000003.11:g.3112263_3112284dup, NC_000003.11:g.3112262_3112284dup, NC_000003.11:g.3112261_3112284dup, NG_029547.1:g.44784_44799del, NG_029547.1:g.44785_44799del, NG_029547.1:g.44787_44799del, NG_029547.1:g.44788_44799del, NG_029547.1:g.44789_44799del, NG_029547.1:g.44790_44799del, NG_029547.1:g.44791_44799del, NG_029547.1:g.44792_44799del, NG_029547.1:g.44793_44799del, NG_029547.1:g.44794_44799del, NG_029547.1:g.44795_44799del, NG_029547.1:g.44796_44799del, NG_029547.1:g.44797_44799del, NG_029547.1:g.44798_44799del, NG_029547.1:g.44799del, NG_029547.1:g.44799dup, NG_029547.1:g.44798_44799dup, NG_029547.1:g.44797_44799dup, NG_029547.1:g.44796_44799dup, NG_029547.1:g.44795_44799dup, NG_029547.1:g.44794_44799dup, NG_029547.1:g.44793_44799dup, NG_029547.1:g.44792_44799dup, NG_029547.1:g.44791_44799dup, NG_029547.1:g.44790_44799dup, NG_029547.1:g.44789_44799dup, NG_029547.1:g.44788_44799dup, NG_029547.1:g.44787_44799dup, NG_029547.1:g.44786_44799dup, NG_029547.1:g.44785_44799dup, NG_029547.1:g.44784_44799dup, NG_029547.1:g.44783_44799dup, NG_029547.1:g.44782_44799dup, NG_029547.1:g.44781_44799dup, NG_029547.1:g.44780_44799dup, NG_029547.1:g.44779_44799dup, NG_029547.1:g.44778_44799dup, NG_029547.1:g.44777_44799dup, NG_029547.1:g.44776_44799dup

Select item 14915361412.

rs1491536141 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:3101178 (GRCh38)
3:3142862 (GRCh37)
Canonical SPDI:: NC_000003.12:3101177:CA:
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.3101178_3101179del, NC_000003.11:g.3142862_3142863del, NG_029547.1:g.14196_14197del

Select item 14915113283.

rs1491511328 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:3096278 (GRCh38)
3:3137962 (GRCh37)
Canonical SPDI:: NC_000003.12:3096277:CA:
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000003.12:g.3096278_3096279del, NC_000003.11:g.3137962_3137963del, NG_029547.1:g.19096_19097del

Select item 14914825384.

rs1491482538 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 3:3107249 (GRCh38)
3:3148934 (GRCh37)
Canonical SPDI:: NC_000003.12:3107249::C
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.3107249_3107250insC, NC_000003.11:g.3148933_3148934insC, NG_029547.1:g.8125_8126insG

Select item 14914676655.

rs1491467665 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 3:3071552 (GRCh38)
3:3113236 (GRCh37)
Canonical SPDI:: NC_000003.12:3071551:AG:
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00177/21 (ALFA)
-=0.000425/7 (TOMMO)
-=0.003453/404 (GnomAD)
HGVS:: NC_000003.12:g.3071552_3071553del, NC_000003.11:g.3113236_3113237del, NG_029547.1:g.43822_43823del

Select item 14914593266.

rs1491459326 has merged into rs113446607 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,TT,TTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 3:3071606 (GRCh38)
3:3113290 (GRCh37)
Canonical SPDI:: NC_000003.12:3071597:TTTTTTTTTTTT:TTTTTTTT,NC_000003.12:3071597:TTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:3071597:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:3071597:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:3071597:TTTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
T=0.0065/108 (TOMMO)
T=0.01378/25 (Korea1K)
HGVS:: NC_000003.12:g.3071606_3071609del, NC_000003.12:g.3071608_3071609del, NC_000003.12:g.3071609del, NC_000003.12:g.3071609dup, NC_000003.12:g.3071608_3071609dup, NC_000003.11:g.3113290_3113293del, NC_000003.11:g.3113292_3113293del, NC_000003.11:g.3113293del, NC_000003.11:g.3113293dup, NC_000003.11:g.3113292_3113293dup, NG_029547.1:g.43774_43777del, NG_029547.1:g.43776_43777del, NG_029547.1:g.43777del, NG_029547.1:g.43777dup, NG_029547.1:g.43776_43777dup

Select item 14914024197.

rs1491402419 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TCAC,TCTCAC [Show Flanks]
Chromosome:: 3:3069659 (GRCh38)
3:3111344 (GRCh37)
Canonical SPDI:: NC_000003.12:3069659:C:CTCAC,NC_000003.12:3069659:C:CTCTCAC
Gene:: IL5RA (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCAC=0./0 (ALFA)
HGVS:: NC_000003.12:g.3069660_3069661insTCAC, NC_000003.12:g.3069660CT[2]CAC[1], NC_000003.11:g.3111344_3111345insTCAC, NC_000003.11:g.3111344CT[2]CAC[1], NG_029547.1:g.45715_45716insTGAG, NG_029547.1:g.45715_45716insTGAGAG, NM_000564.5:c.*565_*566insTGAG, NM_000564.5:c.*565_*566insTGAGAG, NM_000564.4:c.*565_*566insTGAG, NM_000564.4:c.*565_*566insTGAGAG, NM_175726.4:c.*565_*566insTGAG, NM_175726.4:c.*565_*566insTGAGAG, NM_175726.3:c.*565_*566insTGAG, NM_175726.3:c.*565_*566insTGAGAG, NM_001243099.2:c.*606_*607insTGAG, NM_001243099.2:c.*606_*607insTGAGAG, NM_001243099.1:c.*606_*607insTGAG, NM_001243099.1:c.*606_*607insTGAGAG, XM_011533678.3:c.*565_*566insTGAG, XM_011533678.3:c.*565_*566insTGAGAG, XM_011533678.2:c.*565_*566insTGAG, XM_011533678.2:c.*565_*566insTGAGAG, XM_011533678.1:c.*565_*566insTGAG, XM_011533678.1:c.*565_*566insTGAGAG, XM_011533677.2:c.*565_*566insTGAG, XM_011533677.2:c.*565_*566insTGAGAG, XM_011533677.1:c.*565_*566insTGAG, XM_011533677.1:c.*565_*566insTGAGAG

Select item 14912903148.

rs1491290314 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:3078834 (GRCh38)
3:3120518 (GRCh37)
Canonical SPDI:: NC_000003.12:3078833:CA:
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.3078834_3078835del, NC_000003.11:g.3120518_3120519del, NG_029547.1:g.36540_36541del

Select item 14912694389.

rs1491269438 has merged into rs55736610 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 3:3071565 (GRCh38)
3:3113249 (GRCh37)
Canonical SPDI:: NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:3071552:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTGTGT=0./0 (ALFA)
GTGTGTGTGTGTGTGTGTGT=0.025/1 (GENOME_DK)
HGVS:: NC_000003.12:g.3071553GT[6], NC_000003.12:g.3071553GT[7], NC_000003.12:g.3071553GT[8], NC_000003.12:g.3071553GT[9], NC_000003.12:g.3071553GT[10], NC_000003.12:g.3071553GT[11], NC_000003.12:g.3071553GT[12], NC_000003.12:g.3071553GT[13], NC_000003.12:g.3071553GT[14], NC_000003.12:g.3071553GT[15], NC_000003.12:g.3071553GT[16], NC_000003.12:g.3071553GT[17], NC_000003.12:g.3071553GT[18], NC_000003.12:g.3071553GT[19], NC_000003.12:g.3071553GT[20], NC_000003.12:g.3071553GT[21], NC_000003.12:g.3071553GT[23], NC_000003.12:g.3071553GT[24], NC_000003.12:g.3071553GT[25], NC_000003.12:g.3071553GT[26], NC_000003.12:g.3071553GT[27], NC_000003.12:g.3071553GT[28], NC_000003.12:g.3071553GT[29], NC_000003.12:g.3071553GT[30], NC_000003.12:g.3071553GT[31], NC_000003.11:g.3113237GT[6], NC_000003.11:g.3113237GT[7], NC_000003.11:g.3113237GT[8], NC_000003.11:g.3113237GT[9], NC_000003.11:g.3113237GT[10], NC_000003.11:g.3113237GT[11], NC_000003.11:g.3113237GT[12], NC_000003.11:g.3113237GT[13], NC_000003.11:g.3113237GT[14], NC_000003.11:g.3113237GT[15], NC_000003.11:g.3113237GT[16], NC_000003.11:g.3113237GT[17], NC_000003.11:g.3113237GT[18], NC_000003.11:g.3113237GT[19], NC_000003.11:g.3113237GT[20], NC_000003.11:g.3113237GT[21], NC_000003.11:g.3113237GT[23], NC_000003.11:g.3113237GT[24], NC_000003.11:g.3113237GT[25], NC_000003.11:g.3113237GT[26], NC_000003.11:g.3113237GT[27], NC_000003.11:g.3113237GT[28], NC_000003.11:g.3113237GT[29], NC_000003.11:g.3113237GT[30], NC_000003.11:g.3113237GT[31], NG_029547.1:g.43779AC[6], NG_029547.1:g.43779AC[7], NG_029547.1:g.43779AC[8], NG_029547.1:g.43779AC[9], NG_029547.1:g.43779AC[10], NG_029547.1:g.43779AC[11], NG_029547.1:g.43779AC[12], NG_029547.1:g.43779AC[13], NG_029547.1:g.43779AC[14], NG_029547.1:g.43779AC[15], NG_029547.1:g.43779AC[16], NG_029547.1:g.43779AC[17], NG_029547.1:g.43779AC[18], NG_029547.1:g.43779AC[19], NG_029547.1:g.43779AC[20], NG_029547.1:g.43779AC[21], NG_029547.1:g.43779AC[23], NG_029547.1:g.43779AC[24], NG_029547.1:g.43779AC[25], NG_029547.1:g.43779AC[26], NG_029547.1:g.43779AC[27], NG_029547.1:g.43779AC[28], NG_029547.1:g.43779AC[29], NG_029547.1:g.43779AC[30], NG_029547.1:g.43779AC[31]

Select item 149122243210.

rs1491222432 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,G,GTA,GTG,GTGTA,GTGTG,GTGTGTA,GTGTGTG,GTGTGTGTA,GTGTGTGTG,GTGTGTGTGTG [Show Flanks]
Chromosome:: 3:3071598 (GRCh38)
3:3113283 (GRCh37)
Canonical SPDI:: NC_000003.12:3071598::A,NC_000003.12:3071598::G,NC_000003.12:3071598::GTA,NC_000003.12:3071598::GTG,NC_000003.12:3071598::GTGTA,NC_000003.12:3071598::GTGTG,NC_000003.12:3071598::GTGTGTA,NC_000003.12:3071598::GTGTGTG,NC_000003.12:3071598::GTGTGTGTA,NC_000003.12:3071598::GTGTGTGTG,NC_000003.12:3071598::GTGTGTGTGTG
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTA=0./0 (ALFA)
HGVS:: NC_000003.12:g.3071598_3071599insA, NC_000003.12:g.3071598_3071599insG, NC_000003.12:g.3071598_3071599insGTA, NC_000003.12:g.3071598_3071599insGTG, NC_000003.12:g.3071598_3071599insGTGTA, NC_000003.12:g.3071598_3071599insGTGTG, NC_000003.12:g.3071598_3071599insGTGTGTA, NC_000003.12:g.3071598_3071599insGTGTGTG, NC_000003.12:g.3071598_3071599insGTGTGTGTA, NC_000003.12:g.3071598_3071599insGTGTGTGTG, NC_000003.12:g.3071598_3071599insGTGTGTGTGTG, NC_000003.11:g.3113282_3113283insA, NC_000003.11:g.3113282_3113283insG, NC_000003.11:g.3113282_3113283insGTA, NC_000003.11:g.3113282_3113283insGTG, NC_000003.11:g.3113282_3113283insGTGTA, NC_000003.11:g.3113282_3113283insGTGTG, NC_000003.11:g.3113282_3113283insGTGTGTA, NC_000003.11:g.3113282_3113283insGTGTGTG, NC_000003.11:g.3113282_3113283insGTGTGTGTA, NC_000003.11:g.3113282_3113283insGTGTGTGTG, NC_000003.11:g.3113282_3113283insGTGTGTGTGTG, NG_029547.1:g.43776_43777insT, NG_029547.1:g.43776_43777insC, NG_029547.1:g.43776_43777insTAC, NG_029547.1:g.43776_43777insCAC, NG_029547.1:g.43776_43777insTACAC, NG_029547.1:g.43776_43777insCACAC, NG_029547.1:g.43776_43777insTACACAC, NG_029547.1:g.43776_43777insCACACAC, NG_029547.1:g.43776_43777insTACACACAC, NG_029547.1:g.43776_43777insCACACACAC, NG_029547.1:g.43776_43777insCACACACACAC

Select item 149120623711.

rs1491206237 has merged into rs200006367 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT [Show Flanks]
Chromosome:: 3:3089658 (GRCh38)
3:3131342 (GRCh37)
Canonical SPDI:: NC_000003.12:3089646:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:3089646:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:3089646:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:3089646:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:3089646:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: IL5RA (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.07191/43 (NorthernSweden)
HGVS:: NC_000003.12:g.3089658_3089659del, NC_000003.12:g.3089659del, NC_000003.12:g.3089659dup, NC_000003.12:g.3089658_3089659dup, NC_000003.12:g.3089657_3089659dup, NC_000003.11:g.3131342_3131343del, NC_000003.11:g.3131343del, NC_000003.11:g.3131343dup, NC_000003.11:g.3131342_3131343dup, NC_000003.11:g.3131341_3131343dup, NG_029547.1:g.25727_25728del, NG_029547.1:g.25728del, NG_029547.1:g.25728dup, NG_029547.1:g.25727_25728dup, NG_029547.1:g.25726_25728dup

Select item 149118245112.

rs1491182451 has merged into rs3214846 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>-,C,CCC,CCCC,CCCCC,CCCCCC,CCCCCCCC,CCCCCCCCC,CCCCCCCCCC [Show Flanks]
Chromosome:: 3:3105632 (GRCh38)
3:3147316 (GRCh37)
Canonical SPDI:: NC_000003.12:3105624:CCCCCCCCC:CCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCCCC
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCCCCCC=0./0 (ALFA)
C=0.1298/650 (1000Genomes)
HGVS:: NC_000003.12:g.3105632_3105633del, NC_000003.12:g.3105633del, NC_000003.12:g.3105633dup, NC_000003.12:g.3105632_3105633dup, NC_000003.12:g.3105631_3105633dup, NC_000003.12:g.3105630_3105633dup, NC_000003.12:g.3105628_3105633dup, NC_000003.12:g.3105627_3105633dup, NC_000003.12:g.3105626_3105633dup, NC_000003.11:g.3147316_3147317del, NC_000003.11:g.3147317del, NC_000003.11:g.3147317dup, NC_000003.11:g.3147316_3147317dup, NC_000003.11:g.3147315_3147317dup, NC_000003.11:g.3147314_3147317dup, NC_000003.11:g.3147312_3147317dup, NC_000003.11:g.3147311_3147317dup, NC_000003.11:g.3147310_3147317dup, NG_029547.1:g.9749_9750del, NG_029547.1:g.9750del, NG_029547.1:g.9750dup, NG_029547.1:g.9749_9750dup, NG_029547.1:g.9748_9750dup, NG_029547.1:g.9747_9750dup, NG_029547.1:g.9745_9750dup, NG_029547.1:g.9744_9750dup, NG_029547.1:g.9743_9750dup

Select item 149114350213.

rs1491143502 has merged into rs371826442 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 3:3078847 (GRCh38)
3:3120531 (GRCh37)
Canonical SPDI:: NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:3078834:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AAA=0.3954/1980 (1000Genomes)
HGVS:: NC_000003.12:g.3078847_3078853del, NC_000003.12:g.3078848_3078853del, NC_000003.12:g.3078849_3078853del, NC_000003.12:g.3078850_3078853del, NC_000003.12:g.3078851_3078853del, NC_000003.12:g.3078852_3078853del, NC_000003.12:g.3078853del, NC_000003.12:g.3078853dup, NC_000003.12:g.3078852_3078853dup, NC_000003.12:g.3078847_3078853dup, NC_000003.12:g.3078846_3078853dup, NC_000003.11:g.3120531_3120537del, NC_000003.11:g.3120532_3120537del, NC_000003.11:g.3120533_3120537del, NC_000003.11:g.3120534_3120537del, NC_000003.11:g.3120535_3120537del, NC_000003.11:g.3120536_3120537del, NC_000003.11:g.3120537del, NC_000003.11:g.3120537dup, NC_000003.11:g.3120536_3120537dup, NC_000003.11:g.3120531_3120537dup, NC_000003.11:g.3120530_3120537dup, NG_029547.1:g.36534_36540del, NG_029547.1:g.36535_36540del, NG_029547.1:g.36536_36540del, NG_029547.1:g.36537_36540del, NG_029547.1:g.36538_36540del, NG_029547.1:g.36539_36540del, NG_029547.1:g.36540del, NG_029547.1:g.36540dup, NG_029547.1:g.36539_36540dup, NG_029547.1:g.36534_36540dup, NG_029547.1:g.36533_36540dup

Select item 149111078714.

rs1491110787 has merged into rs10606924 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 3:3101191 (GRCh38)
3:3142875 (GRCh37)
Canonical SPDI:: NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:3101178:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
AAA=0.0531/266 (1000Genomes)
HGVS:: NC_000003.12:g.3101191_3101195del, NC_000003.12:g.3101192_3101195del, NC_000003.12:g.3101193_3101195del, NC_000003.12:g.3101194_3101195del, NC_000003.12:g.3101195del, NC_000003.12:g.3101195dup, NC_000003.12:g.3101193_3101195dup, NC_000003.11:g.3142875_3142879del, NC_000003.11:g.3142876_3142879del, NC_000003.11:g.3142877_3142879del, NC_000003.11:g.3142878_3142879del, NC_000003.11:g.3142879del, NC_000003.11:g.3142879dup, NC_000003.11:g.3142877_3142879dup, NG_029547.1:g.14192_14196del, NG_029547.1:g.14193_14196del, NG_029547.1:g.14194_14196del, NG_029547.1:g.14195_14196del, NG_029547.1:g.14196del, NG_029547.1:g.14196dup, NG_029547.1:g.14194_14196dup

Select item 149110937515.

rs1491109375 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 3:3071597 (GRCh38)
3:3113281 (GRCh37)
Canonical SPDI:: NC_000003.12:3071595:TAT:T
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00001/1 (GnomAD)
-=0.05605/216 (ALSPAC)
-=0.06607/245 (TWINSUK)
HGVS:: NC_000003.12:g.3071597_3071598del, NC_000003.11:g.3113281_3113282del, NG_029547.1:g.43778_43779del

Select item 149108354216.

rs1491083542 has merged into rs10642608 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:3075215 (GRCh38)
3:3116899 (GRCh37)
Canonical SPDI:: NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:3075203:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000003.12:g.3075215_3075227del, NC_000003.12:g.3075216_3075227del, NC_000003.12:g.3075217_3075227del, NC_000003.12:g.3075218_3075227del, NC_000003.12:g.3075219_3075227del, NC_000003.12:g.3075220_3075227del, NC_000003.12:g.3075221_3075227del, NC_000003.12:g.3075222_3075227del, NC_000003.12:g.3075223_3075227del, NC_000003.12:g.3075224_3075227del, NC_000003.12:g.3075225_3075227del, NC_000003.12:g.3075226_3075227del, NC_000003.12:g.3075227del, NC_000003.12:g.3075227dup, NC_000003.12:g.3075226_3075227dup, NC_000003.12:g.3075225_3075227dup, NC_000003.12:g.3075224_3075227dup, NC_000003.12:g.3075223_3075227dup, NC_000003.12:g.3075222_3075227dup, NC_000003.12:g.3075221_3075227dup, NC_000003.12:g.3075220_3075227dup, NC_000003.12:g.3075219_3075227dup, NC_000003.12:g.3075218_3075227dup, NC_000003.12:g.3075217_3075227dup, NC_000003.12:g.3075216_3075227dup, NC_000003.12:g.3075215_3075227dup, NC_000003.12:g.3075214_3075227dup, NC_000003.12:g.3075213_3075227dup, NC_000003.12:g.3075212_3075227dup, NC_000003.12:g.3075208_3075227dup, NC_000003.12:g.3075207_3075227dup, NC_000003.12:g.3075205_3075227dup, NC_000003.12:g.3075227_3075228insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.3075227_3075228insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.3075227_3075228insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.3116899_3116911del, NC_000003.11:g.3116900_3116911del, NC_000003.11:g.3116901_3116911del, NC_000003.11:g.3116902_3116911del, NC_000003.11:g.3116903_3116911del, NC_000003.11:g.3116904_3116911del, NC_000003.11:g.3116905_3116911del, NC_000003.11:g.3116906_3116911del, NC_000003.11:g.3116907_3116911del, NC_000003.11:g.3116908_3116911del, NC_000003.11:g.3116909_3116911del, NC_000003.11:g.3116910_3116911del, NC_000003.11:g.3116911del, NC_000003.11:g.3116911dup, NC_000003.11:g.3116910_3116911dup, NC_000003.11:g.3116909_3116911dup, NC_000003.11:g.3116908_3116911dup, NC_000003.11:g.3116907_3116911dup, NC_000003.11:g.3116906_3116911dup, NC_000003.11:g.3116905_3116911dup, NC_000003.11:g.3116904_3116911dup, NC_000003.11:g.3116903_3116911dup, NC_000003.11:g.3116902_3116911dup, NC_000003.11:g.3116901_3116911dup, NC_000003.11:g.3116900_3116911dup, NC_000003.11:g.3116899_3116911dup, NC_000003.11:g.3116898_3116911dup, NC_000003.11:g.3116897_3116911dup, NC_000003.11:g.3116896_3116911dup, NC_000003.11:g.3116892_3116911dup, NC_000003.11:g.3116891_3116911dup, NC_000003.11:g.3116889_3116911dup, NC_000003.11:g.3116911_3116912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.3116911_3116912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.3116911_3116912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029547.1:g.40159_40171del, NG_029547.1:g.40160_40171del, NG_029547.1:g.40161_40171del, NG_029547.1:g.40162_40171del, NG_029547.1:g.40163_40171del, NG_029547.1:g.40164_40171del, NG_029547.1:g.40165_40171del, NG_029547.1:g.40166_40171del, NG_029547.1:g.40167_40171del, NG_029547.1:g.40168_40171del, NG_029547.1:g.40169_40171del, NG_029547.1:g.40170_40171del, NG_029547.1:g.40171del, NG_029547.1:g.40171dup, NG_029547.1:g.40170_40171dup, NG_029547.1:g.40169_40171dup, NG_029547.1:g.40168_40171dup, NG_029547.1:g.40167_40171dup, NG_029547.1:g.40166_40171dup, NG_029547.1:g.40165_40171dup, NG_029547.1:g.40164_40171dup, NG_029547.1:g.40163_40171dup, NG_029547.1:g.40162_40171dup, NG_029547.1:g.40161_40171dup, NG_029547.1:g.40160_40171dup, NG_029547.1:g.40159_40171dup, NG_029547.1:g.40158_40171dup, NG_029547.1:g.40157_40171dup, NG_029547.1:g.40156_40171dup, NG_029547.1:g.40152_40171dup, NG_029547.1:g.40151_40171dup, NG_029547.1:g.40149_40171dup, NG_029547.1:g.40171_40172insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029547.1:g.40171_40172insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029547.1:g.40171_40172insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149108055817.

rs1491080558 has merged into rs5846243 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 3:3107260 (GRCh38)
3:3148944 (GRCh37)
Canonical SPDI:: NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:3107249:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0.0007/4 (ALFA)
T=0.3159/1582 (1000Genomes)
HGVS:: NC_000003.12:g.3107260_3107262del, NC_000003.12:g.3107261_3107262del, NC_000003.12:g.3107262del, NC_000003.12:g.3107262dup, NC_000003.12:g.3107261_3107262dup, NC_000003.12:g.3107260_3107262dup, NC_000003.12:g.3107259_3107262dup, NC_000003.11:g.3148944_3148946del, NC_000003.11:g.3148945_3148946del, NC_000003.11:g.3148946del, NC_000003.11:g.3148946dup, NC_000003.11:g.3148945_3148946dup, NC_000003.11:g.3148944_3148946dup, NC_000003.11:g.3148943_3148946dup, NG_029547.1:g.8123_8125del, NG_029547.1:g.8124_8125del, NG_029547.1:g.8125del, NG_029547.1:g.8125dup, NG_029547.1:g.8124_8125dup, NG_029547.1:g.8123_8125dup, NG_029547.1:g.8122_8125dup

Select item 149106919818.

rs1491069198 has merged into rs3214846 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>-,C,CCC,CCCC,CCCCC,CCCCCC,CCCCCCCC,CCCCCCCCC,CCCCCCCCCC [Show Flanks]
Chromosome:: 3:3105632 (GRCh38)
3:3147316 (GRCh37)
Canonical SPDI:: NC_000003.12:3105624:CCCCCCCCC:CCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCCC,NC_000003.12:3105624:CCCCCCCCC:CCCCCCCCCCCCCCCCC
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCCCCCC=0./0 (ALFA)
C=0.1298/650 (1000Genomes)
HGVS:: NC_000003.12:g.3105632_3105633del, NC_000003.12:g.3105633del, NC_000003.12:g.3105633dup, NC_000003.12:g.3105632_3105633dup, NC_000003.12:g.3105631_3105633dup, NC_000003.12:g.3105630_3105633dup, NC_000003.12:g.3105628_3105633dup, NC_000003.12:g.3105627_3105633dup, NC_000003.12:g.3105626_3105633dup, NC_000003.11:g.3147316_3147317del, NC_000003.11:g.3147317del, NC_000003.11:g.3147317dup, NC_000003.11:g.3147316_3147317dup, NC_000003.11:g.3147315_3147317dup, NC_000003.11:g.3147314_3147317dup, NC_000003.11:g.3147312_3147317dup, NC_000003.11:g.3147311_3147317dup, NC_000003.11:g.3147310_3147317dup, NG_029547.1:g.9749_9750del, NG_029547.1:g.9750del, NG_029547.1:g.9750dup, NG_029547.1:g.9749_9750dup, NG_029547.1:g.9748_9750dup, NG_029547.1:g.9747_9750dup, NG_029547.1:g.9745_9750dup, NG_029547.1:g.9744_9750dup, NG_029547.1:g.9743_9750dup

Select item 149106572819.

rs1491065728 [Homo sapiens]

Variant type:: DELINS
Alleles:: CG>- [Show Flanks]
Chromosome:: 3:3112045 (GRCh38)
3:3153729 (GRCh37)
Canonical SPDI:: NC_000003.12:3112043:GCG:G
Gene:: IL5RA (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00185/22 (ALFA)
-=0.00673/287 (GnomAD)
HGVS:: NC_000003.12:g.3112045_3112046del, NC_000003.11:g.3153729_3153730del, NG_029547.1:g.3330_3331del

Select item 149103886320.

rs1491038863 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 3:3096292 (GRCh38)
3:3137976 (GRCh37)
Canonical SPDI:: NC_000003.12:3096290:AGA:A
Gene:: IL5RA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00143/17 (ALFA)
-=0.00007/0 (TOMMO)
-=0.02013/32 (GnomAD)
HGVS:: NC_000003.12:g.3096292_3096293del, NC_000003.11:g.3137976_3137977del, NG_029547.1:g.19083_19084del

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