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rs746353274

From SNPedia

Orientationplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs746353274(-;-)
Make rs746353274(-;CTT)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position11796341
GeneMTHFR
is asnp
is mentioned by
dbSNPrs746353274
ebirs746353274
HLIrs746353274
Exacrs746353274
Varsomers746353274
Maprs746353274
PheGenIrs746353274
hapmaprs746353274
1000 genomesrs746353274
hgdprs746353274
ensemblrs746353274
gopubmedrs746353274
geneviewrs746353274
scholarrs746353274
googlers746353274
pharmgkbrs746353274
gwascentralrs746353274
openSNPrs746353274
23andMers746353274
23andMe allrs746353274
SNP Nexus

SNPshotrs746353274
SNPdbers746353274
MSV3drs746353274
GWAS Ctlgrs746353274
Max Magnitude0
ClinVar
Risk rs746353274(;)
Alt rs746353274(;)
Reference rs746353274(CTT;CTT)
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.11856398_11856400delCTT
CLNSRC
CLNACC RCV000167598.1,