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rs786205066

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205066(G;T)
Make rs786205066(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68211258
GeneCLN6
is asnp
is mentioned by
dbSNPrs786205066
ebirs786205066
HLIrs786205066
Exacrs786205066
Varsomers786205066
Maprs786205066
PheGenIrs786205066
hapmaprs786205066
1000 genomesrs786205066
hgdprs786205066
ensemblrs786205066
gopubmedrs786205066
geneviewrs786205066
scholarrs786205066
googlers786205066
pharmgkbrs786205066
gwascentralrs786205066
openSNPrs786205066
23andMers786205066
23andMe allrs786205066
SNP Nexus

SNPshotrs786205066
SNPdbers786205066
MSV3drs786205066
GWAS Ctlgrs786205066
Max Magnitude0
ClinVar
Risk rs786205066(T;T)
Alt rs786205066(T;T)
Reference rs786205066(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.68503596C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004300.4,