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rs387906619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906619(C;T)
Make rs387906619(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position80649393
GeneDHFR
is asnp
is mentioned by
dbSNPrs387906619
ebirs387906619
HLIrs387906619
Exacrs387906619
Varsomers387906619
Maprs387906619
PheGenIrs387906619
hapmaprs387906619
1000 genomesrs387906619
hgdprs387906619
ensemblrs387906619
gopubmedrs387906619
geneviewrs387906619
scholarrs387906619
googlers387906619
pharmgkbrs387906619
gwascentralrs387906619
openSNPrs387906619
23andMers387906619
23andMe allrs387906619
SNP Nexus

SNPshotrs387906619
SNPdbers387906619
MSV3drs387906619
GWAS Ctlgrs387906619
Max Magnitude0
ClinVar
Risk rs387906619(T;T)
Alt rs387906619(T;T)
Reference rs387906619(C;C)
Significance Pathogenic
Disease Megaloblastic anemia due to dihydrofolate reductase deficiency
Variation info
Gene DHFR
CLNDBN Megaloblastic anemia due to dihydrofolate reductase deficiency
Reversed 1
HGVS NC_000005.9:g.79945212G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022524.28,