Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515352

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515352(-;-)
Make rs397515352(-;C)
Make rs397515352(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position68211844
GeneCLN6
is asnp
is mentioned by
dbSNPrs397515352
ebirs397515352
HLIrs397515352
Exacrs397515352
Varsomers397515352
Maprs397515352
PheGenIrs397515352
hapmaprs397515352
1000 genomesrs397515352
hgdprs397515352
ensemblrs397515352
gopubmedrs397515352
geneviewrs397515352
scholarrs397515352
googlers397515352
pharmgkbrs397515352
gwascentralrs397515352
openSNPrs397515352
23andMers397515352
23andMe allrs397515352
SNP Nexus

SNPshotrs397515352
SNPdbers397515352
MSV3drs397515352
GWAS Ctlgrs397515352
Max Magnitude0
ClinVar
Risk rs397515352(C;C)
Alt rs397515352(C;C)
Reference rs397515352(;)
Significance Pathogenic
Disease Ceroid lipofuscinosis neuronal 6
Variation info
Gene CLN6
CLNDBN Ceroid lipofuscinosis neuronal 6
Reversed 1
HGVS NC_000015.9:g.68504183dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004296.4,