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rs143781303

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs143781303(C;C)
Make rs143781303(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68208309
GeneCLN6
is asnp
is mentioned by
dbSNPrs143781303
ebirs143781303
HLIrs143781303
Exacrs143781303
Varsomers143781303
Maprs143781303
PheGenIrs143781303
hapmaprs143781303
1000 genomesrs143781303
hgdprs143781303
ensemblrs143781303
gopubmedrs143781303
geneviewrs143781303
scholarrs143781303
googlers143781303
pharmgkbrs143781303
gwascentralrs143781303
openSNPrs143781303
23andMers143781303
23andMe allrs143781303
SNP Nexus

SNPshotrs143781303
SNPdbers143781303
MSV3drs143781303
GWAS Ctlgrs143781303
Max Magnitude0
ClinVar
Risk rs143781303(C;C)
Alt rs143781303(C;C)
Reference rs143781303(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.68500647T>C
CLNSRC
CLNACC RCV000187106.1,