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rs776483190

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776483190(C;T)
Make rs776483190(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position11802980
GeneMTHFR
is asnp
is mentioned by
dbSNPrs776483190
ebirs776483190
HLIrs776483190
Exacrs776483190
Varsomers776483190
Maprs776483190
PheGenIrs776483190
hapmaprs776483190
1000 genomesrs776483190
hgdprs776483190
ensemblrs776483190
gopubmedrs776483190
geneviewrs776483190
scholarrs776483190
googlers776483190
pharmgkbrs776483190
gwascentralrs776483190
openSNPrs776483190
23andMers776483190
23andMe allrs776483190
SNP Nexus

SNPshotrs776483190
SNPdbers776483190
MSV3drs776483190
GWAS Ctlgrs776483190
Max Magnitude0
ClinVar
Risk rs776483190(T;T)
Alt rs776483190(T;T)
Reference rs776483190(C;C)
Significance Pathogenic
Disease Homocysteinemia due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocysteinemia due to MTHFR deficiency
Reversed 0
HGVS NC_000001.10:g.11863037C>T
CLNSRC
CLNACC RCV000167587.1,