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rs796052351

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052351(A;A)
Make rs796052351(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68214289
GeneCLN6
is asnp
is mentioned by
dbSNPrs796052351
ebirs796052351
HLIrs796052351
Exacrs796052351
Varsomers796052351
Maprs796052351
PheGenIrs796052351
hapmaprs796052351
1000 genomesrs796052351
hgdprs796052351
ensemblrs796052351
gopubmedrs796052351
geneviewrs796052351
scholarrs796052351
googlers796052351
pharmgkbrs796052351
gwascentralrs796052351
openSNPrs796052351
23andMers796052351
23andMe allrs796052351
SNP Nexus

SNPshotrs796052351
SNPdbers796052351
MSV3drs796052351
GWAS Ctlgrs796052351
Max Magnitude0
ClinVar
Risk rs796052351(A;A)
Alt rs796052351(A;A)
Reference rs796052351(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68506627C>T
CLNSRC
CLNACC RCV000187092.1,