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: rs376131751
rs376131751
SLC34A1
2 0.925 0.120 5 177396762 missense variant G/C snv 2.8E-05 1.7E-04 0.700 1.000 1 2018 2018