Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs118192177
rs118192177
0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05
Malignant hyperthermia susceptibility type 1
0.800 0
dbSNP: rs118192177
rs118192177
0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05
Malignant hyperpyrexia due to anesthesia
0.720 1.000 8 1998 2015
dbSNP: rs118192177
rs118192177
0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.700 0
dbSNP: rs118192177
rs118192177
0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05
CUI: C0344490
Disease: Sacral agenesis
Sacral agenesis
0.700 0