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rs1064796945

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position23334877
GenePTCHD1
is asnp
is mentioned by
dbSNPrs1064796945
dbSNP (old)rs1064796945
ClinGenrs1064796945
ebirs1064796945
HLIrs1064796945
Exacrs1064796945
Gnomadrs1064796945
Varsomers1064796945
Maprs1064796945
PheGenIrs1064796945
Biobankrs1064796945
1000 genomesrs1064796945
hgdprs1064796945
ensemblrs1064796945
gopubmedrs1064796945
geneviewrs1064796945
scholarrs1064796945
googlers1064796945
pharmgkbrs1064796945
gwascentralrs1064796945
openSNPrs1064796945
23andMers1064796945
23andMe allrs1064796945
SNPshotrs1064796945
SNPdbers1064796945
MSV3drs1064796945
GWAS Ctlgrs1064796945
Max Magnitude0
ClinVar
Risk rs1064796945(C;C)
Alt rs1064796945(C;C)
Reference Rs1064796945(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.23352994T>C
CLNSRC
CLNACC RCV000478083.1,