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rs786204013

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204013(A;C)
Make rs786204013(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11801196
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204013
ebirs786204013
HLIrs786204013
Exacrs786204013
Varsomers786204013
Maprs786204013
PheGenIrs786204013
hapmaprs786204013
1000 genomesrs786204013
hgdprs786204013
ensemblrs786204013
gopubmedrs786204013
geneviewrs786204013
scholarrs786204013
googlers786204013
pharmgkbrs786204013
gwascentralrs786204013
openSNPrs786204013
23andMers786204013
23andMe allrs786204013
SNP Nexus

SNPshotrs786204013
SNPdbers786204013
MSV3drs786204013
GWAS Ctlgrs786204013
Max Magnitude0
ClinVar
Risk rs786204013(C;C)
Alt rs786204013(C;C)
Reference rs786204013(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.11861253T>G
CLNSRC
CLNACC RCV000167595.1,