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rs886039727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039727(A;A)
Make rs886039727(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position68218535
GeneCLN6
is asnp
is mentioned by
dbSNPrs886039727
dbSNP (old)rs886039727
ClinGenrs886039727
ebirs886039727
HLIrs886039727
Exacrs886039727
Varsomers886039727
Maprs886039727
PheGenIrs886039727
Biobankrs886039727
1000 genomesrs886039727
hgdprs886039727
ensemblrs886039727
gopubmedrs886039727
geneviewrs886039727
scholarrs886039727
googlers886039727
pharmgkbrs886039727
gwascentralrs886039727
openSNPrs886039727
23andMers886039727
23andMe allrs886039727
SNP Nexus

SNPshotrs886039727
SNPdbers886039727
MSV3drs886039727
GWAS Ctlgrs886039727
Max Magnitude0
ClinVar
Risk rs886039727(A;A)
Alt rs886039727(A;A)
Reference Rs886039727(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68510873C>T
CLNSRC
CLNACC RCV000255264.1,