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rs150001589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150001589(A;A)
Make rs150001589(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68214309
GeneCLN6
is asnp
is mentioned by
dbSNPrs150001589
ebirs150001589
HLIrs150001589
Exacrs150001589
Varsomers150001589
Maprs150001589
PheGenIrs150001589
hapmaprs150001589
1000 genomesrs150001589
hgdprs150001589
ensemblrs150001589
gopubmedrs150001589
geneviewrs150001589
scholarrs150001589
googlers150001589
pharmgkbrs150001589
gwascentralrs150001589
openSNPrs150001589
23andMers150001589
23andMe allrs150001589
SNP Nexus

SNPshotrs150001589
SNPdbers150001589
MSV3drs150001589
GWAS Ctlgrs150001589
Max Magnitude0
ClinVar
Risk rs150001589(A;A)
Alt rs150001589(A;A)
Reference rs150001589(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene CLN6
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.68506647G>A
CLNSRC
CLNACC RCV000187115.2,