Have questions? Visit https://www.reddit.com/r/SNPedia

rs546989392

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs546989392(C;T)
Make rs546989392(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position76996010
GeneCLN5
is asnp
is mentioned by
dbSNPrs546989392
ebirs546989392
HLIrs546989392
Exacrs546989392
Varsomers546989392
Maprs546989392
PheGenIrs546989392
hapmaprs546989392
1000 genomesrs546989392
hgdprs546989392
ensemblrs546989392
gopubmedrs546989392
geneviewrs546989392
scholarrs546989392
googlers546989392
pharmgkbrs546989392
gwascentralrs546989392
openSNPrs546989392
23andMers546989392
23andMe allrs546989392
SNP Nexus

SNPshotrs546989392
SNPdbers546989392
MSV3drs546989392
GWAS Ctlgrs546989392
Max Magnitude0
ClinVar
Risk rs546989392(T;T)
Alt rs546989392(T;T)
Reference rs546989392(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN5
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.77570145C>T
CLNSRC
CLNACC RCV000187069.1,