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rs769701646

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769701646(C;T)
Make rs769701646(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position68211754
GeneCLN6
is asnp
is mentioned by
dbSNPrs769701646
dbSNP (old)rs769701646
ClinGenrs769701646
ebirs769701646
HLIrs769701646
Exacrs769701646
Gnomadrs769701646
Varsomers769701646
Maprs769701646
PheGenIrs769701646
Biobankrs769701646
1000 genomesrs769701646
hgdprs769701646
ensemblrs769701646
gopubmedrs769701646
geneviewrs769701646
scholarrs769701646
googlers769701646
pharmgkbrs769701646
gwascentralrs769701646
openSNPrs769701646
23andMers769701646
23andMe allrs769701646
SNP Nexus

SNPshotrs769701646
SNPdbers769701646
MSV3drs769701646
GWAS Ctlgrs769701646
Max Magnitude0
ClinVar
Risk rs769701646(T;T)
Alt rs769701646(T;T)
Reference Rs769701646(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene CLN6
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000015.9:g.68504092C>T
CLNSRC
CLNACC RCV000454168.1,