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rs875989785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989785(-;-)
Make rs875989785(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position244054892
GeneZBTB18
is asnp
is mentioned by
dbSNPrs875989785
ebirs875989785
HLIrs875989785
Exacrs875989785
Varsomers875989785
Maprs875989785
PheGenIrs875989785
hapmaprs875989785
1000 genomesrs875989785
hgdprs875989785
ensemblrs875989785
gopubmedrs875989785
geneviewrs875989785
scholarrs875989785
googlers875989785
pharmgkbrs875989785
gwascentralrs875989785
openSNPrs875989785
23andMers875989785
23andMe allrs875989785
SNP Nexus

SNPshotrs875989785
SNPdbers875989785
MSV3drs875989785
GWAS Ctlgrs875989785
Max Magnitude0
ClinVar
Risk rs875989785(;)
Alt rs875989785(;)
Reference rs875989785(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZBTB18
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.244218194delG
CLNSRC
CLNACC RCV000211111.1,