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: rs121917856
rs121917856
IHH ; MIR3131
1 1.000 0.120 2 219060331 missense variant G/A snv 0.800 1.000 1 2003 2003
dbSNP: rs121917857
rs121917857
IHH
1 1.000 0.120 2 219057441 missense variant A/G snv 0.800 1.000 1 2003 2003