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rs398122397

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs398122397(-;-)
Make rs398122397(-;GT)
ReferenceGRCh38 38.1/141
Chromosome8
Position42459925
GeneSLC20A2
is asnp
is mentioned by
dbSNPrs398122397
ebirs398122397
HLIrs398122397
Exacrs398122397
Varsomers398122397
Maprs398122397
PheGenIrs398122397
hapmaprs398122397
1000 genomesrs398122397
hgdprs398122397
ensemblrs398122397
gopubmedrs398122397
geneviewrs398122397
scholarrs398122397
googlers398122397
pharmgkbrs398122397
gwascentralrs398122397
openSNPrs398122397
23andMers398122397
23andMe allrs398122397
SNP Nexus

SNPshotrs398122397
SNPdbers398122397
MSV3drs398122397
GWAS Ctlgrs398122397
Max Magnitude0
ClinVar
Risk rs398122397(;)
Alt rs398122397(;)
Reference rs398122397(GT;GT)
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.42317443_42317444delAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000066208.26,