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rs1064796800

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome16
Position88437537
GeneZNF469
is asnp
is mentioned by
dbSNPrs1064796800
dbSNP (old)rs1064796800
ClinGenrs1064796800
ebirs1064796800
HLIrs1064796800
Exacrs1064796800
Gnomadrs1064796800
Varsomers1064796800
Maprs1064796800
PheGenIrs1064796800
Biobankrs1064796800
1000 genomesrs1064796800
hgdprs1064796800
ensemblrs1064796800
gopubmedrs1064796800
geneviewrs1064796800
scholarrs1064796800
googlers1064796800
pharmgkbrs1064796800
gwascentralrs1064796800
openSNPrs1064796800
23andMers1064796800
23andMe allrs1064796800
SNPshotrs1064796800
SNPdbers1064796800
MSV3drs1064796800
GWAS Ctlgrs1064796800
Max Magnitude0
ClinVar
Risk rs1064796800(G;G)
Alt rs1064796800(G;G)
Reference Rs1064796800(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZNF469
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88503945T>G
CLNSRC
CLNACC RCV000487286.1,