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rs1064793355

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position129829058
GeneZDHHC9
is asnp
is mentioned by
dbSNPrs1064793355
dbSNP (old)rs1064793355
ClinGenrs1064793355
ebirs1064793355
HLIrs1064793355
Exacrs1064793355
Gnomadrs1064793355
Varsomers1064793355
Maprs1064793355
PheGenIrs1064793355
Biobankrs1064793355
1000 genomesrs1064793355
hgdprs1064793355
ensemblrs1064793355
gopubmedrs1064793355
geneviewrs1064793355
scholarrs1064793355
googlers1064793355
pharmgkbrs1064793355
gwascentralrs1064793355
openSNPrs1064793355
23andMers1064793355
23andMe allrs1064793355
SNPshotrs1064793355
SNPdbers1064793355
MSV3drs1064793355
GWAS Ctlgrs1064793355
Max Magnitude0
ClinVar
Risk rs1064793355(C;C)
Alt rs1064793355(C;C)
Reference Rs1064793355(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZDHHC9
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.128963034A>G
CLNSRC
CLNACC RCV000484510.1,