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

rs863224077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs863224077(-;-)
Make rs863224077(-;TG)
Make rs863224077(TG;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position139352682
GeneMRPS22
is asnp
is mentioned by
dbSNPrs863224077
dbSNP (old)rs863224077
ClinGenrs863224077
ebirs863224077
HLIrs863224077
Exacrs863224077
Varsomers863224077
Maprs863224077
PheGenIrs863224077
Biobankrs863224077
1000 genomesrs863224077
hgdprs863224077
ensemblrs863224077
gopubmedrs863224077
geneviewrs863224077
scholarrs863224077
googlers863224077
pharmgkbrs863224077
gwascentralrs863224077
openSNPrs863224077
23andMers863224077
23andMe allrs863224077
SNP Nexus

SNPshotrs863224077
SNPdbers863224077
MSV3drs863224077
GWAS Ctlgrs863224077
Max Magnitude0
ClinVar
Risk rs863224077(-;-)
Alt rs863224077(-;-)
Reference Rs863224077(GT;GT)
Significance Pathogenic
Disease not provided
Variation info
Gene MRPS22
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.139071524_139071525delTG
CLNSRC
CLNACC RCV000199847.1,