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rs797044854

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044854(C;T)
Make rs797044854(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position252459
GeneZMYND11
is asnp
is mentioned by
dbSNPrs797044854
ebirs797044854
HLIrs797044854
Exacrs797044854
Varsomers797044854
Maprs797044854
PheGenIrs797044854
hapmaprs797044854
1000 genomesrs797044854
hgdprs797044854
ensemblrs797044854
gopubmedrs797044854
geneviewrs797044854
scholarrs797044854
googlers797044854
pharmgkbrs797044854
gwascentralrs797044854
openSNPrs797044854
23andMers797044854
23andMe allrs797044854
SNP Nexus

SNPshotrs797044854
SNPdbers797044854
MSV3drs797044854
GWAS Ctlgrs797044854
Max Magnitude0
ClinVar
Risk rs797044854(T;T)
Alt rs797044854(T;T)
Reference rs797044854(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZMYND11
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.298399C>T
CLNSRC
CLNACC RCV000190655.1,