rs1157637439, VARS2

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Acidosis, Lactic
CUI: C0001125
Disease: Acidosis, Lactic
21 0.882 0.120 6 30920187 missense variant A/G snv 0.010 1.000 1 2018 2018
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.120 6 30920187 missense variant A/G snv 0.010 1.000 1 2018 2018
Hypertrophic obstructive cardiomyopathy
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
90 0.882 0.120 6 30920187 missense variant A/G snv 0.010 1.000 1 2018 2018
Persistent Fetal Circulation Syndrome
CUI: C0031190
Disease: Persistent Fetal Circulation Syndrome
7 0.882 0.120 6 30920187 missense variant A/G snv 0.010 1.000 1 2018 2018