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: rs104893873
rs104893873
SLC25A4
1 1.000 0.200 4 185144992 missense variant G/C snv 0.800 1.000 7 2000 2016
dbSNP: rs104893874
rs104893874
SLC25A4
1 1.000 0.200 4 185146939 missense variant G/A snv 0.800 1.000 7 2000 2016
dbSNP: rs104893876
rs104893876
SLC25A4
1 1.000 0.200 4 185144945 missense variant T/C snv 0.800 1.000 7 2000 2016
dbSNP: rs28999114
rs28999114
SLC25A4
2 0.925 0.200 4 185144963 missense variant A/G snv 0.800 1.000 7 2000 2016