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rs1064796787

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome15
Position68218651
GeneCLN6
is asnp
is mentioned by
dbSNPrs1064796787
dbSNP (old)rs1064796787
ClinGenrs1064796787
ebirs1064796787
HLIrs1064796787
Exacrs1064796787
Gnomadrs1064796787
Varsomers1064796787
Maprs1064796787
PheGenIrs1064796787
Biobankrs1064796787
1000 genomesrs1064796787
hgdprs1064796787
ensemblrs1064796787
gopubmedrs1064796787
geneviewrs1064796787
scholarrs1064796787
googlers1064796787
pharmgkbrs1064796787
gwascentralrs1064796787
openSNPrs1064796787
23andMers1064796787
23andMe allrs1064796787
SNPshotrs1064796787
SNPdbers1064796787
MSV3drs1064796787
GWAS Ctlgrs1064796787
Max Magnitude0
ClinVar
Risk rs1064796787(A;A)
Alt rs1064796787(A;A)
Reference Rs1064796787(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68510989C>T
CLNSRC
CLNACC RCV000484435.1,