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rs886041393

From SNPedia
Merged intors398122395
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
is asnp
is mentioned by
dbSNPrs886041393
dbSNP (old)rs886041393
ClinGenrs886041393
ebirs886041393
HLIrs886041393
Exacrs886041393
Gnomadrs886041393
Varsomers886041393
Maprs886041393
PheGenIrs886041393
Biobankrs886041393
1000 genomesrs886041393
hgdprs886041393
ensemblrs886041393
gopubmedrs886041393
geneviewrs886041393
scholarrs886041393
googlers886041393
pharmgkbrs886041393
gwascentralrs886041393
openSNPrs886041393
23andMers886041393
23andMe allrs886041393
SNP Nexus

SNPshotrs886041393
SNPdbers886041393
MSV3drs886041393
GWAS Ctlgrs886041393
StatusMerged into rs398122395
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs886041393(T;T)
Significance Pathogenic
Disease Idiopathic basal ganglia calcification 1 not provided
Variation info
Gene SLC20A2
CLNDBN Idiopathic basal ganglia calcification 1 not provided
Reversed 1
HGVS NC_000008.10:g.42320530delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000066204.26, RCV000303018.1,