Gene: HCG18 ×
Source: GWASDB ×
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: rs928822
rs928822
HCG18 ; HCG17
1 1.000 0.120 6 30307469 intron variant G/T snv 0.66 0.700 1.000 2 2007 2009
dbSNP: rs261949
rs261949
HCG18 ; HCG17
1 1.000 0.120 6 30302303 non coding transcript exon variant G/A snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs9357097
rs9357097
HCG18 ; HCG17
1 1.000 0.120 6 30317344 intron variant C/T snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs9380167
rs9380167
HCG18 ; HCG17
1 1.000 0.120 6 30306684 non coding transcript exon variant A/G snv 0.32 0.700 1.000 1 2009 2009