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rs367585605

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367585605(C;T)
Make rs367585605(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position11794385
GeneMTHFR
is asnp
is mentioned by
dbSNPrs367585605
ebirs367585605
HLIrs367585605
Exacrs367585605
Varsomers367585605
Maprs367585605
PheGenIrs367585605
hapmaprs367585605
1000 genomesrs367585605
hgdprs367585605
ensemblrs367585605
gopubmedrs367585605
geneviewrs367585605
scholarrs367585605
googlers367585605
pharmgkbrs367585605
gwascentralrs367585605
openSNPrs367585605
23andMers367585605
23andMe allrs367585605
SNP Nexus

SNPshotrs367585605
SNPdbers367585605
MSV3drs367585605
GWAS Ctlgrs367585605
Max Magnitude0
ClinVar
Risk rs367585605(T;T)
Alt rs367585605(T;T)
Reference rs367585605(C;C)
Significance Pathogenic
Disease Homocysteinemia due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocysteinemia due to MTHFR deficiency
Reversed 0
HGVS NC_000001.10:g.11854442C>T
CLNSRC
CLNACC RCV000167613.1,