RS112176450 EIF4G1

Health Risk Chr 3:184327400 snv missense variant
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What This Variant Does
"rs112176450, also known as Arg1205His or R1205H, is a SNP in the eukaryotic translation initiation f...
Associated Conditions
Parkinson disease 18
autosomal dominant
susceptibility to
Parkinson disease 18
autosomal dominant
susceptibility to
ClinVar Assertions (1)
NM_198241.3(EIF4G1):c.3614G>A (p.Arg1205His)
· 1 submitter
Population Frequencies
gnomAD ALL
0%
Other Variants in EIF4G1
rs111290936
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