Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs630602
rs630602
SSBP3
1 54263191 intron variant G/C snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2016 2016
dbSNP: rs643428
rs643428
SSBP3
1 54263185 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019