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rs267607167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607167(C;T)
Make rs267607167(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160421171
GeneVANGL2
is asnp
is mentioned by
dbSNPrs267607167
ebirs267607167
HLIrs267607167
Exacrs267607167
Varsomers267607167
Maprs267607167
PheGenIrs267607167
hapmaprs267607167
1000 genomesrs267607167
hgdprs267607167
ensemblrs267607167
gopubmedrs267607167
geneviewrs267607167
scholarrs267607167
googlers267607167
pharmgkbrs267607167
gwascentralrs267607167
openSNPrs267607167
23andMers267607167
23andMe allrs267607167
SNP Nexus

SNPshotrs267607167
SNPdbers267607167
MSV3drs267607167
GWAS Ctlgrs267607167
Max Magnitude0
ClinVar
Risk rs267607167(G,T;G,T)
Alt rs267607167(G,T;G,T)
Reference rs267607167(C;C)
Significance Other
Disease Neural tube defects
Variation info
Gene VANGL2
CLNDBN Neural tube defects, susceptibility to
Reversed 0
HGVS NC_000001.10:g.160390961C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009619.7,