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rs796052354

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052354(A;G)
Make rs796052354(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68211727
GeneCLN6
is asnp
is mentioned by
dbSNPrs796052354
ebirs796052354
HLIrs796052354
Exacrs796052354
Varsomers796052354
Maprs796052354
PheGenIrs796052354
hapmaprs796052354
1000 genomesrs796052354
hgdprs796052354
ensemblrs796052354
gopubmedrs796052354
geneviewrs796052354
scholarrs796052354
googlers796052354
pharmgkbrs796052354
gwascentralrs796052354
openSNPrs796052354
23andMers796052354
23andMe allrs796052354
SNP Nexus

SNPshotrs796052354
SNPdbers796052354
MSV3drs796052354
GWAS Ctlgrs796052354
Max Magnitude0
ClinVar
Risk rs796052354(G;G)
Alt rs796052354(G;G)
Reference rs796052354(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68504065T>C
CLNSRC
CLNACC RCV000187098.1,