Gene: HMGCR ×
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: rs12916
rs12916
HMGCR ; CERT1
3 0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 0.800 1.000 3 2010 2019
dbSNP: rs3846662
rs3846662
HMGCR
5 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.800 1.000 2 2009 2019
dbSNP: rs10038095
rs10038095
HMGCR
3 5 75341886 intron variant A/T snv 0.38 0.800 1.000 1 2012 2019
dbSNP: rs10045497
rs10045497
HMGCR
1 5 75340659 intron variant C/A snv 0.35 0.800 1.000 1 2013 2013
dbSNP: rs12654264
rs12654264
HMGCR
5 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.800 1.000 1 2012 2019
dbSNP: rs10474434
rs10474434
HMGCR
3 5 75348856 intron variant G/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs17238484
rs17238484
HMGCR
3 1.000 0.080 5 75352671 intron variant G/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs3761739
rs3761739
HMGCR
3 5 75335676 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs6453131
rs6453131
HMGCR
3 5 75348881 intron variant T/G snv 0.39 0.700 1.000 1 2012 2012