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: rs137852814
rs137852814
16 0.752 0.240 2 39022774 missense variant T/A;C snv 4.0E-06 0.700 0
dbSNP: rs397517148
rs397517148
27 0.776 0.200 2 39023128 missense variant C/T snv 0.700 0
dbSNP: rs397517150
rs397517150
7 0.827 0.160 2 39023118 missense variant A/C;G snv 0.700 0
dbSNP: rs727505381
rs727505381
5 0.925 0.160 2 39013523 missense variant A/G snv 4.0E-06 0.700 0