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rs267606887

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606887(A;G)
Make rs267606887(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11795158
GeneMTHFR
is asnp
is mentioned by
dbSNPrs267606887
ebirs267606887
HLIrs267606887
Exacrs267606887
Varsomers267606887
Maprs267606887
PheGenIrs267606887
hapmaprs267606887
1000 genomesrs267606887
hgdprs267606887
ensemblrs267606887
gopubmedrs267606887
geneviewrs267606887
scholarrs267606887
googlers267606887
pharmgkbrs267606887
gwascentralrs267606887
openSNPrs267606887
23andMers267606887
23andMe allrs267606887
SNP Nexus

SNPshotrs267606887
SNPdbers267606887
MSV3drs267606887
GWAS Ctlgrs267606887
Max Magnitude0
ClinVar
Risk rs267606887(G;G)
Alt rs267606887(G;G)
Reference rs267606887(A;A)
Significance Pathogenic
Disease Homocystinuria due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocystinuria due to MTHFR deficiency
Reversed 1
HGVS NC_000001.10:g.11855215T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003700.2,