CLDN14, claudin 14, 23562

N. diseases: 36; N. variants: 17
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: rs170183
rs170183
21 36476036 intron variant G/A snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2014 2014
dbSNP: rs7277076
rs7277076
1.000 0.080 21 36464675 intron variant T/C snv 0.52
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018