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rs139365610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139365610(C;T)
Make rs139365610(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position49807348
GeneAP2A1, FUZ
is asnp
is mentioned by
dbSNPrs139365610
ebirs139365610
HLIrs139365610
Exacrs139365610
Varsomers139365610
Maprs139365610
PheGenIrs139365610
hapmaprs139365610
1000 genomesrs139365610
hgdprs139365610
ensemblrs139365610
gopubmedrs139365610
geneviewrs139365610
scholarrs139365610
googlers139365610
pharmgkbrs139365610
gwascentralrs139365610
openSNPrs139365610
23andMers139365610
23andMe allrs139365610
SNP Nexus

SNPshotrs139365610
SNPdbers139365610
MSV3drs139365610
GWAS Ctlgrs139365610
Max Magnitude0
ClinVar
Risk rs139365610(A,T;A,T)
Alt rs139365610(A,T;A,T)
Reference rs139365610(C;C)
Significance Other
Disease Neural tube defects
Variation info
Gene FUZ AP2A1
CLNDBN Neural tube defects, susceptibility to
Reversed 0
HGVS NC_000019.9:g.50310605C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024614.4,