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rs483353068

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483353068(C;C)
Make rs483353068(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position114339426
GeneZBTB20
is asnp
is mentioned by
dbSNPrs483353068
ebirs483353068
HLIrs483353068
Exacrs483353068
Varsomers483353068
Maprs483353068
PheGenIrs483353068
hapmaprs483353068
1000 genomesrs483353068
hgdprs483353068
ensemblrs483353068
gopubmedrs483353068
geneviewrs483353068
scholarrs483353068
googlers483353068
pharmgkbrs483353068
gwascentralrs483353068
openSNPrs483353068
23andMers483353068
23andMe allrs483353068
SNP Nexus

SNPshotrs483353068
SNPdbers483353068
MSV3drs483353068
GWAS Ctlgrs483353068
Max Magnitude0
ClinVar
Risk rs483353068(C;C)
Alt rs483353068(C;C)
Reference rs483353068(G;G)
Significance Pathogenic
Disease Primrose syndrome
Variation info
Gene ZBTB20
CLNDBN Primrose syndrome
Reversed 1
HGVS NC_000003.11:g.114058273C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000133614.4,