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: rs16917546
rs16917546
ZNF365 ; LOC105378327
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2018 2019
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2017 2017