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: rs74315291
rs74315291
CHRNB2
3 0.882 0.080 1 154571682 missense variant G/A;C;T snv 0.800 1.000 2 2000 2001
dbSNP: rs1064796396
rs1064796396
CHRNB2
1 1.000 0.040 1 154572114 missense variant G/C snv 3.0E-05 7.0E-06 0.700 0
dbSNP: rs281865067
rs281865067
CHRNA4
1 1.000 0.040 20 63350538 inframe insertion -/CAG delins 0.700 0
dbSNP: rs281865072
rs281865072
CHRNB2
1 1.000 0.040 1 154571833 missense variant T/A;G snv 4.0E-06; 4.0E-06 0.700 0