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rs796052338

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052338(A;A)
Make rs796052338(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position28477577
GeneCLN3, NPIPB8
is asnp
is mentioned by
dbSNPrs796052338
ebirs796052338
HLIrs796052338
Exacrs796052338
Varsomers796052338
Maprs796052338
PheGenIrs796052338
hapmaprs796052338
1000 genomesrs796052338
hgdprs796052338
ensemblrs796052338
gopubmedrs796052338
geneviewrs796052338
scholarrs796052338
googlers796052338
pharmgkbrs796052338
gwascentralrs796052338
openSNPrs796052338
23andMers796052338
23andMe allrs796052338
SNP Nexus

SNPshotrs796052338
SNPdbers796052338
MSV3drs796052338
GWAS Ctlgrs796052338
Max Magnitude0
ClinVar
Risk rs796052338(A;A)
Alt rs796052338(A;A)
Reference Rs796052338(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPIPB8 CLN3
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.28488898C>T
CLNSRC
CLNACC RCV000187023.1,