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rs886041533

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome19
Position7527563
GeneMCOLN1
is asnp
is mentioned by
dbSNPrs886041533
dbSNP (classic)rs886041533
ClinGenrs886041533
ebirs886041533
HLIrs886041533
Exacrs886041533
Gnomadrs886041533
Varsomers886041533
LitVarrs886041533
Maprs886041533
PheGenIrs886041533
Biobankrs886041533
1000 genomesrs886041533
hgdprs886041533
ensemblrs886041533
geneviewrs886041533
scholarrs886041533
googlers886041533
pharmgkbrs886041533
gwascentralrs886041533
openSNPrs886041533
23andMers886041533
23andMe allrs886041533
SNPshotrs886041533
SNPdbers886041533
MSV3drs886041533
GWAS Ctlgrs886041533
Max Magnitude0
ClinVar
Risk rs886041533(C;C)
Alt rs886041533(C;C)
Reference Rs886041533(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MCOLN1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.7592449dupC
CLNSRC
CLNACC RCV000368147.1,