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rs786204037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204037(C;C)
Make rs786204037(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11790768
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204037
dbSNP (old)rs786204037
ClinGenrs786204037
ebirs786204037
HLIrs786204037
Exacrs786204037
Varsomers786204037
Maprs786204037
PheGenIrs786204037
Biobankrs786204037
1000 genomesrs786204037
hgdprs786204037
ensemblrs786204037
gopubmedrs786204037
geneviewrs786204037
scholarrs786204037
googlers786204037
pharmgkbrs786204037
gwascentralrs786204037
openSNPrs786204037
23andMers786204037
23andMe allrs786204037
SNP Nexus

SNPshotrs786204037
SNPdbers786204037
MSV3drs786204037
GWAS Ctlgrs786204037
Max Magnitude0
ClinVar
Risk rs786204037(C;C)
Alt rs786204037(C;C)
Reference Rs786204037(T;T)
Significance Pathogenic
Disease Homocysteinemia due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocysteinemia due to MTHFR deficiency
Reversed 1
HGVS NC_000001.10:g.11850825A>G
CLNSRC UniProtKB (protein)
CLNACC RCV000167625.1,