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rs387906653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906653(A;A)
Make rs387906653(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position42428829
GeneSLC20A2
is asnp
is mentioned by
dbSNPrs387906653
ebirs387906653
HLIrs387906653
Exacrs387906653
Varsomers387906653
Maprs387906653
PheGenIrs387906653
hapmaprs387906653
1000 genomesrs387906653
hgdprs387906653
ensemblrs387906653
gopubmedrs387906653
geneviewrs387906653
scholarrs387906653
googlers387906653
pharmgkbrs387906653
gwascentralrs387906653
openSNPrs387906653
23andMers387906653
23andMe allrs387906653
SNP Nexus

SNPshotrs387906653
SNPdbers387906653
MSV3drs387906653
GWAS Ctlgrs387906653
Max Magnitude0
ClinVar
Risk rs387906653(A;A)
Alt rs387906653(A;A)
Reference rs387906653(G;G)
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.42286347C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022665.26,