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rs796052355

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052355(C;C)
Make rs796052355(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68211673
GeneCLN6
is asnp
is mentioned by
dbSNPrs796052355
ebirs796052355
HLIrs796052355
Exacrs796052355
Varsomers796052355
Maprs796052355
PheGenIrs796052355
hapmaprs796052355
1000 genomesrs796052355
hgdprs796052355
ensemblrs796052355
gopubmedrs796052355
geneviewrs796052355
scholarrs796052355
googlers796052355
pharmgkbrs796052355
gwascentralrs796052355
openSNPrs796052355
23andMers796052355
23andMe allrs796052355
SNP Nexus

SNPshotrs796052355
SNPdbers796052355
MSV3drs796052355
GWAS Ctlgrs796052355
Max Magnitude0
ClinVar
Risk rs796052355(C;C)
Alt rs796052355(C;C)
Reference rs796052355(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68504011A>G
CLNSRC
CLNACC RCV000187099.1,