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rs267607168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607168(C;C)
Make rs267607168(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160425122
GeneVANGL2
is asnp
is mentioned by
dbSNPrs267607168
ebirs267607168
HLIrs267607168
Exacrs267607168
Varsomers267607168
Maprs267607168
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1000 genomesrs267607168
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23andMe allrs267607168
SNP Nexus

SNPshotrs267607168
SNPdbers267607168
MSV3drs267607168
GWAS Ctlgrs267607168
Max Magnitude0
ClinVar
Risk rs267607168(C;C)
Alt rs267607168(C;C)
Reference rs267607168(T;T)
Significance Other
Disease Neural tube defects
Variation info
Gene VANGL2
CLNDBN Neural tube defects, susceptibility to
Reversed 0
HGVS NC_000001.10:g.160394912T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009620.5,