HPN, hepsin, 3249

N. diseases: 57; N. variants: 9
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: rs4806073
rs4806073
19 35064286 intron variant T/C snv 0.85
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.800 1.000 1 2012 2012
dbSNP: rs1688043
rs1688043
19 35062437 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2018 2018