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: rs387907090
rs387907090
RASL12 ; KBTBD13
2 0.925 0.080 15 65078037 missense variant C/A;T snv 0.800 1.000 2 2010 2012
dbSNP: rs200549195
rs200549195
RASL12 ; KBTBD13
1 1.000 0.080 15 65077557 missense variant C/A;T snv 2.0E-05; 4.1E-04 0.800 1.000 1 2012 2012
dbSNP: rs1303411209
rs1303411209
RASL12 ; KBTBD13
1 1.000 0.080 15 65077059 missense variant G/A snv 0.700 0
dbSNP: rs760601340
rs760601340
RASL12 ; KBTBD13
1 1.000 0.080 15 65077841 stop gained T/C;G snv 4.2E-06 0.700 0
dbSNP: rs767384093
rs767384093
RASL12 ; KBTBD13
1 1.000 0.080 15 65077105 missense variant T/C snv 7.4E-05 4.9E-05 0.700 0