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: rs10732995
rs10732995
TNN
1 1 175142438 intron variant C/T snv 0.98 0.700 1.000 1 2019 2019
dbSNP: rs141456816
rs141456816
MYH4 ; MYHAS
1 17 10458990 intron variant T/C snv 8.2E-03 0.700 1.000 1 2019 2019
dbSNP: rs16991615
rs16991615
MCM8
6 0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs186783371
rs186783371
MEF2C
1 5 88766406 non coding transcript exon variant A/T snv 7.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs35829351
rs35829351 		1 11 6099456 intergenic variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs62236881
rs62236881
ZNRF3
1 22 29054205 3 prime UTR variant G/A snv 1.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs62237617
rs62237617
TTC28
3 22 28365160 intron variant C/G;T snv 1.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs7168070
rs7168070
LOC105370982
1 15 93366991 intron variant T/C snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs76673357
rs76673357
LOC107985440
1 20 17850562 intergenic variant T/G snv 7.8E-02 0.700 1.000 1 2019 2019