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rs875989786

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989786(C;T)
Make rs875989786(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position244054957
GeneZBTB18
is asnp
is mentioned by
dbSNPrs875989786
ebirs875989786
HLIrs875989786
Exacrs875989786
Varsomers875989786
Maprs875989786
PheGenIrs875989786
hapmaprs875989786
1000 genomesrs875989786
hgdprs875989786
ensemblrs875989786
gopubmedrs875989786
geneviewrs875989786
scholarrs875989786
googlers875989786
pharmgkbrs875989786
gwascentralrs875989786
openSNPrs875989786
23andMers875989786
23andMe allrs875989786
SNP Nexus

SNPshotrs875989786
SNPdbers875989786
MSV3drs875989786
GWAS Ctlgrs875989786
Max Magnitude0
ClinVar
Risk rs875989786(T;T)
Alt rs875989786(T;T)
Reference rs875989786(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZBTB18
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.244218259C>T
CLNSRC
CLNACC RCV000211094.1,