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rs150263896

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150263896(C;T)
Make rs150263896(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position114339010
GeneZBTB20
is asnp
is mentioned by
dbSNPrs150263896
ebirs150263896
HLIrs150263896
Exacrs150263896
Varsomers150263896
Maprs150263896
PheGenIrs150263896
hapmaprs150263896
1000 genomesrs150263896
hgdprs150263896
ensemblrs150263896
gopubmedrs150263896
geneviewrs150263896
scholarrs150263896
googlers150263896
pharmgkbrs150263896
gwascentralrs150263896
openSNPrs150263896
23andMers150263896
23andMe allrs150263896
SNP Nexus

SNPshotrs150263896
SNPdbers150263896
MSV3drs150263896
GWAS Ctlgrs150263896
Max Magnitude0
ClinVar
Risk rs150263896(T;T)
Alt rs150263896(T;T)
Reference rs150263896(C;C)
Significance Pathogenic
Disease Primrose syndrome
Variation info
Gene ZBTB20
CLNDBN Primrose syndrome
Reversed 0
HGVS NC_000003.11:g.114057857C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239523.1,