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rs121434318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434318(A;A)
Make rs121434318(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position38299471
GeneSPRED1
is asnp
is mentioned by
dbSNPrs121434318
ebirs121434318
HLIrs121434318
Exacrs121434318
Varsomers121434318
Maprs121434318
PheGenIrs121434318
hapmaprs121434318
1000 genomesrs121434318
hgdprs121434318
ensemblrs121434318
gopubmedrs121434318
geneviewrs121434318
scholarrs121434318
googlers121434318
pharmgkbrs121434318
gwascentralrs121434318
openSNPrs121434318
23andMers121434318
23andMe allrs121434318
SNP Nexus

SNPshotrs121434318
SNPdbers121434318
MSV3drs121434318
GWAS Ctlgrs121434318
Max Magnitude0
OMIM609291
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121434318(A;A)
Alt rs121434318(A;A)
Reference rs121434318(T;T)
Significance Pathogenic
Disease Legius syndrome
Variation info
Gene SPRED1
CLNDBN Legius syndrome
Reversed 0
HGVS NC_000015.9:g.38591672T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001889.2,