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rs786204024

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204024(A;G)
Make rs786204024(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11794781
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204024
ebirs786204024
HLIrs786204024
Exacrs786204024
Varsomers786204024
Maprs786204024
PheGenIrs786204024
hapmaprs786204024
1000 genomesrs786204024
hgdprs786204024
ensemblrs786204024
gopubmedrs786204024
geneviewrs786204024
scholarrs786204024
googlers786204024
pharmgkbrs786204024
gwascentralrs786204024
openSNPrs786204024
23andMers786204024
23andMe allrs786204024
SNP Nexus

SNPshotrs786204024
SNPdbers786204024
MSV3drs786204024
GWAS Ctlgrs786204024
Max Magnitude0
ClinVar
Risk rs786204024(G;G)
Alt rs786204024(G;G)
Reference rs786204024(A;A)
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.11854838T>C
CLNSRC
CLNACC RCV000167610.1,