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: rs374664941
rs374664941
ITGA8
1 1.000 0.120 10 15644210 missense variant C/T snv 2.4E-05 2.1E-05 0.800 0
dbSNP: rs587777281
rs587777281
ITGA8
1 1.000 0.120 10 15672662 missense variant G/A;T snv 2.0E-05 0.700 1.000 1 2014 2014
dbSNP: rs587777279
rs587777279
ITGA8
1 1.000 0.120 10 15531048 splice donor variant A/G snv 0.700 0
dbSNP: rs587777280
rs587777280
ITGA8
1 1.000 0.120 10 15607815 frameshift variant ACCTC/- delins 0.700 0
dbSNP: rs748467820
rs748467820
ITGA8
1 1.000 0.120 10 15684035 missense variant G/A;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs79658334
rs79658334
RET
29 0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 0.700 0