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: rs377767404
rs377767404
RET
11 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 1 1999 1999
dbSNP: rs377767429
rs377767429
RET
7 0.790 0.120 10 43120120 missense variant GC/TT mnv 0.700 1.000 1 1999 1999
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.700 1.000 1 1995 1995
dbSNP: rs75076352
rs75076352
RET
24 0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 0.700 1.000 1 1995 1995
dbSNP: rs75234356
rs75234356
RET
14 0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 0.700 1.000 1 2005 2005
dbSNP: rs75996173
rs75996173
RET
21 0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 0.700 1.000 1 1995 1995
dbSNP: rs76262710
rs76262710
RET
17 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.700 1.000 1 1999 1999
dbSNP: rs77503355
rs77503355
RET
8 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.700 1.000 1 1997 1997
dbSNP: rs77709286
rs77709286
RET
12 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.700 1.000 1 1995 1995
dbSNP: rs77724903
rs77724903
RET
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 1.000 1 2005 2005
dbSNP: rs77939446
rs77939446
RET
15 0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 1999 1999
dbSNP: rs78014899
rs78014899
RET
12 0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 0.700 1.000 1 1997 1997
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 1.000 1 1997 1997
dbSNP: rs79781594
rs79781594
RET
16 0.732 0.160 10 43113649 missense variant G/A;C;T snv 0.700 1.000 1 1999 1999
dbSNP: rs1060500186
rs1060500186
CDKN1B ; GPR19
1 1.000 0.120 12 12717887 frameshift variant GACG/- delins 0.700 0
dbSNP: rs121917832
rs121917832
CDKN1B ; GPR19
3 0.925 0.200 12 12718066 stop gained G/A snv 0.700 0
dbSNP: rs1555085575
rs1555085575
CDKN1B ; GPR19
1 1.000 0.120 12 12718118 frameshift variant -/C delins 0.700 0
dbSNP: rs532903617
rs532903617
CDKN1B ; GPR19
1 1.000 0.120 12 12718106 stop gained C/G;T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs774454456
rs774454456
CDKN1B ; GPR19
2 0.925 0.120 12 12717808 5 prime UTR variant AGAG/- delins 3.8E-04 3.8E-04 0.700 0
dbSNP: rs777354267
rs777354267
CDKN1B ; GPR19
2 1.000 0.120 12 12718045 missense variant C/T snv 4.0E-06 2.1E-05 0.700 0
dbSNP: rs786201007
rs786201007
CDKN1B ; GPR19
1 1.000 0.120 12 12717896 frameshift variant -/AGGCGGAGCACCCCAAGCC delins 0.700 0
dbSNP: rs786201010
rs786201010
CDKN1B ; GPR19
1 1.000 0.120 12 12717384 5 prime UTR variant TTCC/- delins 0.700 0
dbSNP: rs786201011
rs786201011
CDKN1B ; GPR19
1 1.000 0.120 12 12718211 frameshift variant CT/- delins 0.700 0