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rs61504484

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61504484(A;A)
Make rs61504484(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position76992067
GeneCLN5
is asnp
is mentioned by
dbSNPrs61504484
ebirs61504484
HLIrs61504484
Exacrs61504484
Varsomers61504484
Maprs61504484
PheGenIrs61504484
hapmaprs61504484
1000 genomesrs61504484
hgdprs61504484
ensemblrs61504484
gopubmedrs61504484
geneviewrs61504484
scholarrs61504484
googlers61504484
pharmgkbrs61504484
gwascentralrs61504484
openSNPrs61504484
23andMers61504484
23andMe allrs61504484
SNP Nexus

SNPshotrs61504484
SNPdbers61504484
MSV3drs61504484
GWAS Ctlgrs61504484
Max Magnitude0
ClinVar
Risk rs61504484(A,G,T;A,G,T)
Alt rs61504484(A,G,T;A,G,T)
Reference rs61504484(C;C)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene CLN5
CLNDBN not provided not specified
Reversed 0
HGVS NC_000013.10:g.77566202C>A; NC_000013.10:g.77566202C>G
CLNSRC
CLNACC RCV000187063.1, RCV000187047.2,