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rs121918220

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918220(C;C)
Make rs121918220(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115683980
GeneVANGL1
is asnp
is mentioned by
dbSNPrs121918220
ebirs121918220
HLIrs121918220
Exacrs121918220
Varsomers121918220
Maprs121918220
PheGenIrs121918220
hapmaprs121918220
1000 genomesrs121918220
hgdprs121918220
ensemblrs121918220
gopubmedrs121918220
geneviewrs121918220
scholarrs121918220
googlers121918220
pharmgkbrs121918220
gwascentralrs121918220
openSNPrs121918220
23andMers121918220
23andMe allrs121918220
SNP Nexus

SNPshotrs121918220
SNPdbers121918220
MSV3drs121918220
GWAS Ctlgrs121918220
Max Magnitude0
OMIM610132
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918220(C;C)
Alt rs121918220(C;C)
Reference rs121918220(T;T)
Significance Other
Disease Neural tube defects
Variation info
Gene VANGL1
CLNDBN Neural tube defects, susceptibility to
Reversed 0
HGVS NC_000001.10:g.116226601T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001413.4,