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rs786204018

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204018(G;T)
Make rs786204018(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11796222
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204018
ebirs786204018
HLIrs786204018
Exacrs786204018
Varsomers786204018
Maprs786204018
PheGenIrs786204018
hapmaprs786204018
1000 genomesrs786204018
hgdprs786204018
ensemblrs786204018
gopubmedrs786204018
geneviewrs786204018
scholarrs786204018
googlers786204018
pharmgkbrs786204018
gwascentralrs786204018
openSNPrs786204018
23andMers786204018
23andMe allrs786204018
SNP Nexus

SNPshotrs786204018
SNPdbers786204018
MSV3drs786204018
GWAS Ctlgrs786204018
Max Magnitude0
ClinVar
Risk rs786204018(T;T)
Alt rs786204018(T;T)
Reference Rs786204018(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.11856279C>A
CLNSRC UniProtKB (protein)
CLNACC RCV000167602.1,