WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Hematocrit procedure ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9330813
rs9330813 		1.000 0.040 22 45968281 intron variant G/A;C snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016