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: rs387907256
rs387907256
SLC17A3
1 6 25850541 missense variant A/G snv 0.700 0
dbSNP: rs387907257
rs387907257
SLC17A3
1 6 25862334 missense variant T/G snv 0.700 0