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rs796052335

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052335(C;T)
Make rs796052335(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position28482340
GeneCLN3, NPIPB8
is asnp
is mentioned by
dbSNPrs796052335
ebirs796052335
HLIrs796052335
Exacrs796052335
Varsomers796052335
Maprs796052335
PheGenIrs796052335
hapmaprs796052335
1000 genomesrs796052335
hgdprs796052335
ensemblrs796052335
gopubmedrs796052335
geneviewrs796052335
scholarrs796052335
googlers796052335
pharmgkbrs796052335
gwascentralrs796052335
openSNPrs796052335
23andMers796052335
23andMe allrs796052335
SNP Nexus

SNPshotrs796052335
SNPdbers796052335
MSV3drs796052335
GWAS Ctlgrs796052335
Max Magnitude0
ClinVar
Risk rs796052335(T;T)
Alt rs796052335(T;T)
Reference rs796052335(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN3 NPIPB8
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.28493661G>A
CLNSRC
CLNACC RCV000187013.1,