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rs786204019

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204019(G;G)
Make rs786204019(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11796217
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204019
ebirs786204019
HLIrs786204019
Exacrs786204019
Varsomers786204019
Maprs786204019
PheGenIrs786204019
hapmaprs786204019
1000 genomesrs786204019
hgdprs786204019
ensemblrs786204019
gopubmedrs786204019
geneviewrs786204019
scholarrs786204019
googlers786204019
pharmgkbrs786204019
gwascentralrs786204019
openSNPrs786204019
23andMers786204019
23andMe allrs786204019
SNP Nexus

SNPshotrs786204019
SNPdbers786204019
MSV3drs786204019
GWAS Ctlgrs786204019
Max Magnitude0
ClinVar
Risk rs786204019(G;G)
Alt rs786204019(G;G)
Reference rs786204019(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.11856274A>C
CLNSRC
CLNACC RCV000167604.1,