Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10554589
rs10554589
ANKRD11 ; LOC105371414
16 89295870 intron variant ATGTG/- delins 0.83
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs117984432
rs117984432
ANKRD11
1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs140088599
rs140088599
ANKRD11
16 89374136 intron variant C/G snv 1.1E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs3114908
rs3114908
ANKRD11
16 89317317 intron variant T/C snv 0.68
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs55637757
rs55637757
ANKRD11
16 89469480 intron variant C/T snv 9.8E-02
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018