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rs797044885

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044885(A;G)
Make rs797044885(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position244055156
GeneZBTB18
is asnp
is mentioned by
dbSNPrs797044885
ebirs797044885
HLIrs797044885
Exacrs797044885
Varsomers797044885
Maprs797044885
PheGenIrs797044885
hapmaprs797044885
1000 genomesrs797044885
hgdprs797044885
ensemblrs797044885
gopubmedrs797044885
geneviewrs797044885
scholarrs797044885
googlers797044885
pharmgkbrs797044885
gwascentralrs797044885
openSNPrs797044885
23andMers797044885
23andMe allrs797044885
SNP Nexus

SNPshotrs797044885
SNPdbers797044885
MSV3drs797044885
GWAS Ctlgrs797044885
Max Magnitude0
ClinVar
Risk rs797044885(G;G)
Alt rs797044885(G;G)
Reference rs797044885(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZBTB18
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.244218458A>G
CLNSRC
CLNACC RCV000190707.1,