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rs796052356

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052356(A;A)
Make rs796052356(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68209636
GeneCLN6
is asnp
is mentioned by
dbSNPrs796052356
ebirs796052356
HLIrs796052356
Exacrs796052356
Varsomers796052356
Maprs796052356
PheGenIrs796052356
hapmaprs796052356
1000 genomesrs796052356
hgdprs796052356
ensemblrs796052356
gopubmedrs796052356
geneviewrs796052356
scholarrs796052356
googlers796052356
pharmgkbrs796052356
gwascentralrs796052356
openSNPrs796052356
23andMers796052356
23andMe allrs796052356
SNP Nexus

SNPshotrs796052356
SNPdbers796052356
MSV3drs796052356
GWAS Ctlgrs796052356
Max Magnitude0
ClinVar
Risk rs796052356(A;A)
Alt rs796052356(A;A)
Reference rs796052356(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68501974C>T
CLNSRC
CLNACC RCV000187100.2,