Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1035650739
rs1035650739
NR1H2 ; NAPSA ; LOC105372437
1 1.000 0.040 19 50362252 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2016 2016