HMCN1, hemicentin 1, 83872

N. diseases: 28; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16824658
rs16824658
0.925 0.040 1 185895380 intron variant A/G snv 7.6E-02
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis
Digestive System Diseases 0.700 1.000 1 2007 2007