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rs777661576

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777661576(C;T)
Make rs777661576(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position11790916
GeneMTHFR
is asnp
is mentioned by
dbSNPrs777661576
ebirs777661576
HLIrs777661576
Exacrs777661576
Varsomers777661576
Maprs777661576
PheGenIrs777661576
hapmaprs777661576
1000 genomesrs777661576
hgdprs777661576
ensemblrs777661576
gopubmedrs777661576
geneviewrs777661576
scholarrs777661576
googlers777661576
pharmgkbrs777661576
gwascentralrs777661576
openSNPrs777661576
23andMers777661576
23andMe allrs777661576
SNP Nexus

SNPshotrs777661576
SNPdbers777661576
MSV3drs777661576
GWAS Ctlgrs777661576
Max Magnitude0
ClinVar
Risk rs777661576(T;T)
Alt rs777661576(T;T)
Reference rs777661576(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.11850973C>T
CLNSRC
CLNACC RCV000167621.1,