Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796052345(-;-)
Make rs796052345(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position77000959
GeneCLN5, FBXL3
is asnp
is mentioned by
dbSNPrs796052345
dbSNP (old)rs796052345
ClinGenrs796052345
ebirs796052345
HLIrs796052345
Exacrs796052345
Varsomers796052345
Maprs796052345
PheGenIrs796052345
Biobankrs796052345
1000 genomesrs796052345
hgdprs796052345
ensemblrs796052345
gopubmedrs796052345
geneviewrs796052345
scholarrs796052345
googlers796052345
pharmgkbrs796052345
gwascentralrs796052345
openSNPrs796052345
23andMers796052345
23andMe allrs796052345
SNP Nexus

SNPshotrs796052345
SNPdbers796052345
MSV3drs796052345
GWAS Ctlgrs796052345
Max Magnitude0
ClinVar
Risk rs796052345(-;-)
Alt rs796052345(-;-)
Reference Rs796052345(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN5
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.77575094_77575095delCT
CLNSRC
CLNACC RCV000187074.1,