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

rs147277149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147277149(C;T)
Make rs147277149(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position7895749
GeneMTRR
is asnp
is mentioned by
dbSNPrs147277149
dbSNP (old)rs147277149
ClinGenrs147277149
ebirs147277149
HLIrs147277149
Exacrs147277149
Gnomadrs147277149
Varsomers147277149
LitVarrs147277149
Maprs147277149
PheGenIrs147277149
Biobankrs147277149
1000 genomesrs147277149
hgdprs147277149
ensemblrs147277149
gopubmedrs147277149
geneviewrs147277149
scholarrs147277149
googlers147277149
pharmgkbrs147277149
gwascentralrs147277149
openSNPrs147277149
23andMers147277149
23andMe allrs147277149
SNPshotrs147277149
SNPdbers147277149
MSV3drs147277149
GWAS Ctlgrs147277149
Max Magnitude0
ClinVar
Risk rs147277149(T;T)
Alt rs147277149(T;T)
Reference Rs147277149(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MTRR
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.7895862C>T
CLNSRC
CLNACC RCV000254795.1,