Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204022

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204022(C;T)
Make rs786204022(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11794835
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204022
ebirs786204022
HLIrs786204022
Exacrs786204022
Varsomers786204022
Maprs786204022
PheGenIrs786204022
hapmaprs786204022
1000 genomesrs786204022
hgdprs786204022
ensemblrs786204022
gopubmedrs786204022
geneviewrs786204022
scholarrs786204022
googlers786204022
pharmgkbrs786204022
gwascentralrs786204022
openSNPrs786204022
23andMers786204022
23andMe allrs786204022
SNP Nexus

SNPshotrs786204022
SNPdbers786204022
MSV3drs786204022
GWAS Ctlgrs786204022
Max Magnitude0
ClinVar
Risk rs786204022(T;T)
Alt rs786204022(T;T)
Reference rs786204022(C;C)
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.11854892G>A
CLNSRC
CLNACC RCV000167608.1,