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: rs1060499761
rs1060499761
1 14 87934803 missense variant A/C snv 0.700 0
dbSNP: rs11300320
rs11300320
1 14 87950752 intron variant AA/-;A;AAA delins 0.96 0.700 0