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rs483353066

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353066(A;G)
Make rs483353066(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position114350291
GeneZBTB20, ZBTB20-AS1
is asnp
is mentioned by
dbSNPrs483353066
ebirs483353066
HLIrs483353066
Exacrs483353066
Varsomers483353066
Maprs483353066
PheGenIrs483353066
hapmaprs483353066
1000 genomesrs483353066
hgdprs483353066
ensemblrs483353066
gopubmedrs483353066
geneviewrs483353066
scholarrs483353066
googlers483353066
pharmgkbrs483353066
gwascentralrs483353066
openSNPrs483353066
23andMers483353066
23andMe allrs483353066
SNP Nexus

SNPshotrs483353066
SNPdbers483353066
MSV3drs483353066
GWAS Ctlgrs483353066
Max Magnitude0
ClinVar
Risk rs483353066(G;G)
Alt rs483353066(G;G)
Reference rs483353066(A;A)
Significance Pathogenic
Disease Primrose syndrome
Variation info
Gene ZBTB20 ZBTB20-AS1
CLNDBN Primrose syndrome
Reversed 1
HGVS NC_000003.11:g.114069138T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133612.4,