Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4663109 2 127164716 intergenic variant A/G snv 0.78 2
rs4510165 2 127178708 intergenic variant C/T snv 0.10 2
rs4284778
CYP27C1
2 127188750 intron variant T/C snv 0.13 2
rs4284779
CYP27C1
2 127188924 intron variant T/C snv 0.13 2
rs4321325
CYP27C1
2 127193421 intron variant C/T snv 0.17 2
rs7568070
CYP27C1
2 127195478 synonymous variant A/C snv 0.26 0.32 2
rs11683427
CYP27C1
2 127198967 intron variant A/G snv 0.22 2
rs11890243
CYP27C1
2 127200465 intron variant C/A;G snv 0.74 2
rs7585314
CYP27C1
2 127204917 intron variant T/A;C snv 2
rs4560059
CYP27C1
2 127214652 intron variant T/C;G snv 2
rs4662710
CYP27C1
2 127219241 intron variant C/G snv 0.40 2
rs1504136
CYP27C1
2 127219542 intron variant T/C snv 0.68 2
rs7567389 2 127225069 upstream gene variant A/T snv 0.67 2
rs1566822 2 127229815 intergenic variant A/G snv 0.40 2
rs6738690 2 127235149 intergenic variant T/C snv 0.77 2
rs4662713 2 127236527 intergenic variant C/A;T snv 2
rs1604817 2 127242345 upstream gene variant C/T snv 0.61 2
rs4536600 2 127244996 upstream gene variant G/A snv 0.59 2
rs2174270 2 127248502 non coding transcript exon variant C/G;T snv 2
rs12465955 2 127249498 non coding transcript exon variant A/G;T snv 2
rs6430936 2 127250110 downstream gene variant A/C snv 0.77 2
rs4662717 2 127255928 downstream gene variant C/T snv 0.47 2
rs4662718
ERCC3
2 127257791 intron variant C/T snv 0.74 2
rs1566823
ERCC3
2 127260616 non coding transcript exon variant A/G snv 0.37 2
rs4150496
ERCC3
2 127271927 intron variant C/A;T snv 0.35 2