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rs786205434

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205434(A;C)
Make rs786205434(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position114339420
GeneZBTB20
is asnp
is mentioned by
dbSNPrs786205434
ebirs786205434
HLIrs786205434
Exacrs786205434
Varsomers786205434
Maprs786205434
PheGenIrs786205434
hapmaprs786205434
1000 genomesrs786205434
hgdprs786205434
ensemblrs786205434
gopubmedrs786205434
geneviewrs786205434
scholarrs786205434
googlers786205434
pharmgkbrs786205434
gwascentralrs786205434
openSNPrs786205434
23andMers786205434
23andMe allrs786205434
SNP Nexus

SNPshotrs786205434
SNPdbers786205434
MSV3drs786205434
GWAS Ctlgrs786205434
Max Magnitude0
ClinVar
Risk rs786205434(C;C)
Alt rs786205434(C;C)
Reference rs786205434(A;A)
Significance Pathogenic
Disease Primrose syndrome Multiple congenital anomalies
Variation info
Gene ZBTB20
CLNDBN Primrose syndrome Multiple congenital anomalies
Reversed 1
HGVS NC_000003.11:g.114058267T>G
CLNSRC
CLNACC RCV000149434.1, RCV000190703.1,