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rs1064796899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position23022189
GeneRBBP8
is asnp
is mentioned by
dbSNPrs1064796899
dbSNP (old)rs1064796899
ClinGenrs1064796899
ebirs1064796899
HLIrs1064796899
Exacrs1064796899
Gnomadrs1064796899
Varsomers1064796899
Maprs1064796899
PheGenIrs1064796899
Biobankrs1064796899
1000 genomesrs1064796899
hgdprs1064796899
ensemblrs1064796899
gopubmedrs1064796899
geneviewrs1064796899
scholarrs1064796899
googlers1064796899
pharmgkbrs1064796899
gwascentralrs1064796899
openSNPrs1064796899
23andMers1064796899
23andMe allrs1064796899
SNPshotrs1064796899
SNPdbers1064796899
MSV3drs1064796899
GWAS Ctlgrs1064796899
Max Magnitude0
ClinVar
Risk rs1064796899(T;T)
Alt rs1064796899(T;T)
Reference Rs1064796899(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBBP8
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.20602152C>T
CLNSRC
CLNACC RCV000480286.1,