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rs398122395

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122395(-;-)
Make rs398122395(-;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position42463013
GeneSLC20A2
is asnp
is mentioned by
dbSNPrs398122395
ebirs398122395
HLIrs398122395
Exacrs398122395
Varsomers398122395
Maprs398122395
PheGenIrs398122395
hapmaprs398122395
1000 genomesrs398122395
hgdprs398122395
ensemblrs398122395
gopubmedrs398122395
geneviewrs398122395
scholarrs398122395
googlers398122395
pharmgkbrs398122395
gwascentralrs398122395
openSNPrs398122395
23andMers398122395
23andMe allrs398122395
SNP Nexus

SNPshotrs398122395
SNPdbers398122395
MSV3drs398122395
GWAS Ctlgrs398122395
Max Magnitude0
ClinVar
Risk rs398122395(;)
Alt rs398122395(;)
Reference rs398122395(T;T)
Significance Pathogenic
Disease Idiopathic basal ganglia calcification 1
Variation info
Gene SLC20A2
CLNDBN Idiopathic basal ganglia calcification 1
Reversed 1
HGVS NC_000008.10:g.42320531delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000066204.26,