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: rs10818854
rs10818854
DENND1A
6 0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 0.010 1.000 1 2015 2015
dbSNP: rs12478601
rs12478601
THADA
5 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.010 1.000 1 2015 2015
dbSNP: rs13405728
rs13405728
LHCGR ; STON1-GTF2A1L
8 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2015 2015
dbSNP: rs13429458
rs13429458
THADA
6 0.827 0.200 2 43411699 intron variant A/C snv 0.14 0.010 1.000 1 2015 2015
dbSNP: rs2059807
rs2059807
INSR
7 0.851 0.200 19 7166098 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs4385527
rs4385527
AOPEP
6 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015
dbSNP: rs6165
rs6165
FSHR
14 0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 0.010 1.000 1 2014 2014
dbSNP: rs6166
rs6166
FSHR
17 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2014 2014