CLDN14, claudin 14, 23562

N. diseases: 36; N. variants: 17
Disease: Hematocrit procedure ×
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: rs128494
rs128494 		21 36461960 intron variant T/C snv 0.72
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016