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rs34181110

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34181110(A;A)
Make rs34181110(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position64425752
GeneMTHFD1
is asnp
is mentioned by
dbSNPrs34181110
dbSNP (old)rs34181110
ClinGenrs34181110
ebirs34181110
HLIrs34181110
Exacrs34181110
Varsomers34181110
Maprs34181110
PheGenIrs34181110
Biobankrs34181110
1000 genomesrs34181110
hgdprs34181110
ensemblrs34181110
gopubmedrs34181110
geneviewrs34181110
scholarrs34181110
googlers34181110
pharmgkbrs34181110
gwascentralrs34181110
openSNPrs34181110
23andMers34181110
23andMe allrs34181110
SNP Nexus

SNPshotrs34181110
SNPdbers34181110
MSV3drs34181110
GWAS Ctlgrs34181110
Max Magnitude0
OMIM172460
Desc
Variant0001
Relatedalso


ClinVar
Risk rs34181110(A;A)
Alt rs34181110(A;A)
Reference Rs34181110(G;G)
Significance Other
Disease Spina bifida
Variation info
Gene MTHFD1
CLNDBN Spina bifida, folate-sensitive, susceptibility to
Reversed 0
HGVS NC_000014.8:g.64892470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014602.2,