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: rs775911275
rs775911275
SLC20A2
1 1.000 0.080 8 42465863 missense variant G/A snv 7.0E-06 0.700 1.000 8 2005 2014