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rs1064796807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position34916789
GeneAPIP, PDHX
is asnp
is mentioned by
dbSNPrs1064796807
dbSNP (old)rs1064796807
ClinGenrs1064796807
ebirs1064796807
HLIrs1064796807
Exacrs1064796807
Gnomadrs1064796807
Varsomers1064796807
LitVarrs1064796807
Maprs1064796807
PheGenIrs1064796807
Biobankrs1064796807
1000 genomesrs1064796807
hgdprs1064796807
ensemblrs1064796807
gopubmedrs1064796807
geneviewrs1064796807
scholarrs1064796807
googlers1064796807
pharmgkbrs1064796807
gwascentralrs1064796807
openSNPrs1064796807
23andMers1064796807
23andMe allrs1064796807
SNPshotrs1064796807
SNPdbers1064796807
MSV3drs1064796807
GWAS Ctlgrs1064796807
Max Magnitude0
ClinVar
Risk rs1064796807(A;A)
Alt rs1064796807(A;A)
Reference Rs1064796807(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDHX APIP
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.34938336G>A
CLNSRC
CLNACC RCV000486323.1,