Have questions? Visit https://www.reddit.com/r/SNPedia

rs147739245

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147739245(C;T)
Make rs147739245(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position139352701
GeneMRPS22
is asnp
is mentioned by
dbSNPrs147739245
ebirs147739245
HLIrs147739245
Exacrs147739245
Varsomers147739245
Maprs147739245
PheGenIrs147739245
hapmaprs147739245
1000 genomesrs147739245
hgdprs147739245
ensemblrs147739245
gopubmedrs147739245
geneviewrs147739245
scholarrs147739245
googlers147739245
pharmgkbrs147739245
gwascentralrs147739245
openSNPrs147739245
23andMers147739245
23andMe allrs147739245
SNP Nexus

SNPshotrs147739245
SNPdbers147739245
MSV3drs147739245
GWAS Ctlgrs147739245
Max Magnitude0
ClinVar
Risk rs147739245(T;T)
Alt rs147739245(T;T)
Reference rs147739245(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPS22
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.139071543C>T
CLNSRC
CLNACC RCV000198671.1,