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rs786204012

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204012(C;C)
Make rs786204012(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11801248
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204012
ebirs786204012
HLIrs786204012
Exacrs786204012
Varsomers786204012
Maprs786204012
PheGenIrs786204012
hapmaprs786204012
1000 genomesrs786204012
hgdprs786204012
ensemblrs786204012
gopubmedrs786204012
geneviewrs786204012
scholarrs786204012
googlers786204012
pharmgkbrs786204012
gwascentralrs786204012
openSNPrs786204012
23andMers786204012
23andMe allrs786204012
SNP Nexus

SNPshotrs786204012
SNPdbers786204012
MSV3drs786204012
GWAS Ctlgrs786204012
Max Magnitude0
ClinVar
Risk rs786204012(C;C)
Alt rs786204012(C;C)
Reference rs786204012(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.11861305A>G
CLNSRC
CLNACC RCV000167594.1,