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: rs104893844
rs104893844
GNRHR ; UBA6-AS1
4 0.882 0.160 4 67754068 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2012 2012
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: rs771470596
rs771470596
EDNRA
4 0.882 0.200 4 147539919 missense variant G/A;C snv 1.6E-05 0.010 1.000 1 2012 2012