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: rs587779752
rs587779752
3 0.882 0.120 7 156791474 intron variant G/A snv 7.0E-06 0.700 0
dbSNP: rs606231149
rs606231149
2 0.925 0.120 7 156791547 intron variant A/G snv 0.700 0
dbSNP: rs606231150
rs606231150
2 0.925 0.120 7 156791137 intron variant T/C snv 0.700 0
dbSNP: rs606231151
rs606231151
2 0.925 0.120 7 156791255 intron variant G/C snv 0.700 0
dbSNP: rs606231152
rs606231152
2 0.925 0.120 7 156791581 intron variant A/G;T snv 0.700 0