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: rs63749888
rs63749888
SLC9B1 ; CISD2
1 1.000 0.200 4 102885221 missense variant G/C snv 0.700 0
dbSNP: rs200599829
rs200599829
AMACR ; C1QTNF3-AMACR
1 1.000 0.200 5 34004665 missense variant G/C snv 8.0E-06 0.010 1.000 1 2017 2017