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rs121918219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918219(A;A)
Make rs121918219(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position115682372
GeneVANGL1
is asnp
is mentioned by
dbSNPrs121918219
ebirs121918219
HLIrs121918219
Exacrs121918219
Varsomers121918219
Maprs121918219
PheGenIrs121918219
hapmaprs121918219
1000 genomesrs121918219
hgdprs121918219
ensemblrs121918219
gopubmedrs121918219
geneviewrs121918219
scholarrs121918219
googlers121918219
pharmgkbrs121918219
gwascentralrs121918219
openSNPrs121918219
23andMers121918219
23andMe allrs121918219
SNP Nexus

SNPshotrs121918219
SNPdbers121918219
MSV3drs121918219
GWAS Ctlgrs121918219
Max Magnitude0
OMIM610132
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918219(A;A)
Alt rs121918219(A;A)
Reference rs121918219(G;G)
Significance Other
Disease Neural tube defects
Variation info
Gene VANGL1
CLNDBN Neural tube defects, susceptibility to
Reversed 0
HGVS NC_000001.10:g.116224993G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001412.4,