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: rs104894275
rs104894275
PTS
3 0.882 0.120 11 112228665 missense variant A/G snv 1.2E-04 7.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs104894276
rs104894276
PTS
3 0.882 0.120 11 112233178 missense variant C/G;T snv 4.0E-06; 7.6E-05 0.010 1.000 1 2001 2001