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rs1064794776

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position49638787
GeneZNF423
is asnp
is mentioned by
dbSNPrs1064794776
dbSNP (old)rs1064794776
ClinGenrs1064794776
ebirs1064794776
HLIrs1064794776
Exacrs1064794776
Gnomadrs1064794776
Varsomers1064794776
LitVarrs1064794776
Maprs1064794776
PheGenIrs1064794776
Biobankrs1064794776
1000 genomesrs1064794776
hgdprs1064794776
ensemblrs1064794776
gopubmedrs1064794776
geneviewrs1064794776
scholarrs1064794776
googlers1064794776
pharmgkbrs1064794776
gwascentralrs1064794776
openSNPrs1064794776
23andMers1064794776
23andMe allrs1064794776
SNPshotrs1064794776
SNPdbers1064794776
MSV3drs1064794776
GWAS Ctlgrs1064794776
Max Magnitude0
ClinVar
Risk rs1064794776(T;T)
Alt rs1064794776(T;T)
Reference Rs1064794776(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZNF423
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.49672698C>A
CLNSRC
CLNACC RCV000485145.1,