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rs786204020

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204020(G;T)
Make rs786204020(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11796205
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204020
ebirs786204020
HLIrs786204020
Exacrs786204020
Varsomers786204020
Maprs786204020
PheGenIrs786204020
hapmaprs786204020
1000 genomesrs786204020
hgdprs786204020
ensemblrs786204020
gopubmedrs786204020
geneviewrs786204020
scholarrs786204020
googlers786204020
pharmgkbrs786204020
gwascentralrs786204020
openSNPrs786204020
23andMers786204020
23andMe allrs786204020
SNP Nexus

SNPshotrs786204020
SNPdbers786204020
MSV3drs786204020
GWAS Ctlgrs786204020
Max Magnitude0
ClinVar
Risk rs786204020(T;T)
Alt rs786204020(T;T)
Reference rs786204020(G;G)
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.11856262C>A
CLNSRC
CLNACC RCV000167605.1,