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rs387907204

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907204(C;T)
Make rs387907204(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position49812733
GeneFUZ
is asnp
is mentioned by
dbSNPrs387907204
ebirs387907204
HLIrs387907204
Exacrs387907204
Varsomers387907204
Maprs387907204
PheGenIrs387907204
hapmaprs387907204
1000 genomesrs387907204
hgdprs387907204
ensemblrs387907204
gopubmedrs387907204
geneviewrs387907204
scholarrs387907204
googlers387907204
pharmgkbrs387907204
gwascentralrs387907204
openSNPrs387907204
23andMers387907204
23andMe allrs387907204
SNP Nexus

SNPshotrs387907204
SNPdbers387907204
MSV3drs387907204
GWAS Ctlgrs387907204
Max Magnitude0
ClinVar
Risk rs387907204(T;T)
Alt rs387907204(T;T)
Reference rs387907204(C;C)
Significance Other
Disease Neural tube defects
Variation info
Gene FUZ
CLNDBN Neural tube defects, susceptibility to
Reversed 1
HGVS NC_000019.9:g.50315990G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024613.6,