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rs543016186

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs543016186(C;T)
Make rs543016186(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11795125
GeneMTHFR
is asnp
is mentioned by
dbSNPrs543016186
ebirs543016186
HLIrs543016186
Exacrs543016186
Varsomers543016186
Maprs543016186
PheGenIrs543016186
hapmaprs543016186
1000 genomesrs543016186
hgdprs543016186
ensemblrs543016186
gopubmedrs543016186
geneviewrs543016186
scholarrs543016186
googlers543016186
pharmgkbrs543016186
gwascentralrs543016186
openSNPrs543016186
23andMers543016186
23andMe allrs543016186
SNP Nexus

SNPshotrs543016186
SNPdbers543016186
MSV3drs543016186
GWAS Ctlgrs543016186
Max Magnitude0
ClinVar
Risk rs543016186(T;T)
Alt rs543016186(T;T)
Reference rs543016186(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.11855182C>T
CLNSRC
CLNACC RCV000167606.1,