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rs786205065

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205065(-;-)
Make rs786205065(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68229578
GeneCLN6
is asnp
is mentioned by
dbSNPrs786205065
ebirs786205065
HLIrs786205065
Exacrs786205065
Varsomers786205065
Maprs786205065
PheGenIrs786205065
hapmaprs786205065
1000 genomesrs786205065
hgdprs786205065
ensemblrs786205065
gopubmedrs786205065
geneviewrs786205065
scholarrs786205065
googlers786205065
pharmgkbrs786205065
gwascentralrs786205065
openSNPrs786205065
23andMers786205065
23andMe allrs786205065
SNP Nexus

SNPshotrs786205065
SNPdbers786205065
MSV3drs786205065
GWAS Ctlgrs786205065
Max Magnitude0
ClinVar
Risk rs786205065(;)
Alt rs786205065(;)
Reference rs786205065(G;G)
Significance Pathogenic
Disease Ceroid lipofuscinosis neuronal 6
Variation info
Gene CLN6
CLNDBN Ceroid lipofuscinosis neuronal 6
Reversed 1
HGVS NC_000015.9:g.68521916delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000004295.4,