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rs121918218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918218(A;A)
Make rs121918218(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position115664171
GeneVANGL1
is asnp
is mentioned by
dbSNPrs121918218
ebirs121918218
HLIrs121918218
Exacrs121918218
Varsomers121918218
Maprs121918218
PheGenIrs121918218
hapmaprs121918218
1000 genomesrs121918218
hgdprs121918218
ensemblrs121918218
gopubmedrs121918218
geneviewrs121918218
scholarrs121918218
googlers121918218
pharmgkbrs121918218
gwascentralrs121918218
openSNPrs121918218
23andMers121918218
23andMe allrs121918218
SNP Nexus

SNPshotrs121918218
SNPdbers121918218
MSV3drs121918218
GWAS Ctlgrs121918218
Max Magnitude0
OMIM610132
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918218(A;A)
Alt rs121918218(A;A)
Reference rs121918218(G;G)
Significance Pathogenic
Disease Caudal regression syndrome
Variation info
Gene VANGL1
CLNDBN Caudal regression syndrome
Reversed 0
HGVS NC_000001.10:g.116206792G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001411.2,