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rs768422260

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGG;AGG) 0 common in clinvar
Make rs768422260(-;-)
Make rs768422260(-;GGA)
Make rs768422260(GGA;GGA)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position68208280
GeneCLN6
is asnp
is mentioned by
dbSNPrs768422260
ClinGenrs768422260
ebirs768422260
HLIrs768422260
Exacrs768422260
Varsomers768422260
Maprs768422260
PheGenIrs768422260
hapmaprs768422260
1000 genomesrs768422260
hgdprs768422260
ensemblrs768422260
gopubmedrs768422260
geneviewrs768422260
scholarrs768422260
googlers768422260
pharmgkbrs768422260
gwascentralrs768422260
openSNPrs768422260
23andMers768422260
23andMe allrs768422260
SNP Nexus

SNPshotrs768422260
SNPdbers768422260
MSV3drs768422260
GWAS Ctlgrs768422260
Max Magnitude0
ClinVar
Risk rs768422260(-;-)
Alt rs768422260(-;-)
Reference Rs768422260(AGG;AGG)
Significance Pathogenic
Disease not specified Ceroid lipofuscinosis neuronal 6
Variation info
Gene CLN6
CLNDBN not specified Ceroid lipofuscinosis neuronal 6
Reversed 0
HGVS NC_000015.9:g.68500618_68500620delAGG
CLNSRC
CLNACC RCV000187114.1, RCV000195031.1,