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: rs1003346
rs1003346
TMEM245
2 1.000 9 109053060 intron variant C/A snv 0.43 0.010 1.000 1 2013 2013
dbSNP: rs151091899
rs151091899
TRPV3
1 1.000 17 3541092 intron variant G/A snv 1.6E-04 0.010 1.000 1 2016 2016
dbSNP: rs12932445
rs12932445
ZFHX3
3 0.925 0.080 16 73035989 intron variant T/C snv 0.18 0.700 1.000 1 2018 2018