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rs154774640

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs154774640(C;G)
Make rs154774640(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position68218584
GeneCLN6
is asnp
is mentioned by
dbSNPrs154774640
dbSNP (old)rs154774640
ClinGenrs154774640
ebirs154774640
HLIrs154774640
Exacrs154774640
Gnomadrs154774640
Varsomers154774640
Maprs154774640
PheGenIrs154774640
Biobankrs154774640
1000 genomesrs154774640
hgdprs154774640
ensemblrs154774640
gopubmedrs154774640
geneviewrs154774640
scholarrs154774640
googlers154774640
pharmgkbrs154774640
gwascentralrs154774640
openSNPrs154774640
23andMers154774640
23andMe allrs154774640
SNPshotrs154774640
SNPdbers154774640
MSV3drs154774640
GWAS Ctlgrs154774640
Max Magnitude0
ClinVar
Risk rs154774640(G;G)
Alt rs154774640(G;G)
Reference Rs154774640(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68510922G>C
CLNSRC
CLNACC RCV000058908.1,