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rs796052336

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052336(A;T)
Make rs796052336(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position28482324
GeneCLN3, NPIPB8
is asnp
is mentioned by
dbSNPrs796052336
ebirs796052336
HLIrs796052336
Exacrs796052336
Varsomers796052336
Maprs796052336
PheGenIrs796052336
hapmaprs796052336
1000 genomesrs796052336
hgdprs796052336
ensemblrs796052336
gopubmedrs796052336
geneviewrs796052336
scholarrs796052336
googlers796052336
pharmgkbrs796052336
gwascentralrs796052336
openSNPrs796052336
23andMers796052336
23andMe allrs796052336
SNP Nexus

SNPshotrs796052336
SNPdbers796052336
MSV3drs796052336
GWAS Ctlgrs796052336
Max Magnitude0
ClinVar
Risk rs796052336(T;T)
Alt rs796052336(T;T)
Reference rs796052336(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN3 NPIPB8
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.28493645T>A
CLNSRC
CLNACC RCV000187014.1,