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rs796052352

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052352(A;A)
Make rs796052352(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68211857
GeneCLN6
is asnp
is mentioned by
dbSNPrs796052352
ebirs796052352
HLIrs796052352
Exacrs796052352
Varsomers796052352
Maprs796052352
PheGenIrs796052352
hapmaprs796052352
1000 genomesrs796052352
hgdprs796052352
ensemblrs796052352
gopubmedrs796052352
geneviewrs796052352
scholarrs796052352
googlers796052352
pharmgkbrs796052352
gwascentralrs796052352
openSNPrs796052352
23andMers796052352
23andMe allrs796052352
SNP Nexus

SNPshotrs796052352
SNPdbers796052352
MSV3drs796052352
GWAS Ctlgrs796052352
Max Magnitude0
ClinVar
Risk rs796052352(A;A)
Alt rs796052352(A;A)
Reference rs796052352(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68504195C>T
CLNSRC
CLNACC RCV000187093.1,