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rs1004428835

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1004428835(C;T)
Make rs1004428835(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position88427489
GeneZNF469
is asnp
is mentioned by
dbSNPrs1004428835
dbSNP (old)rs1004428835
ClinGenrs1004428835
ebirs1004428835
HLIrs1004428835
Exacrs1004428835
Gnomadrs1004428835
Varsomers1004428835
Maprs1004428835
PheGenIrs1004428835
Biobankrs1004428835
1000 genomesrs1004428835
hgdprs1004428835
ensemblrs1004428835
gopubmedrs1004428835
geneviewrs1004428835
scholarrs1004428835
googlers1004428835
pharmgkbrs1004428835
gwascentralrs1004428835
openSNPrs1004428835
23andMers1004428835
23andMe allrs1004428835
SNPshotrs1004428835
SNPdbers1004428835
MSV3drs1004428835
GWAS Ctlgrs1004428835
Max Magnitude0
ClinVar
Risk rs1004428835(T;T)
Alt rs1004428835(T;T)
Reference Rs1004428835(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZNF469
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88493897C>T
CLNSRC
CLNACC RCV000443600.1,