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rs146170087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs146170087(C;C)
Make rs146170087(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position29702747
GeneC19orf12
is asnp
is mentioned by
dbSNPrs146170087
ebirs146170087
HLIrs146170087
Exacrs146170087
Varsomers146170087
Maprs146170087
PheGenIrs146170087
hapmaprs146170087
1000 genomesrs146170087
hgdprs146170087
ensemblrs146170087
gopubmedrs146170087
geneviewrs146170087
scholarrs146170087
googlers146170087
pharmgkbrs146170087
gwascentralrs146170087
openSNPrs146170087
23andMers146170087
23andMe allrs146170087
SNP Nexus

SNPshotrs146170087
SNPdbers146170087
MSV3drs146170087
GWAS Ctlgrs146170087
Max Magnitude0
ClinVar
Risk rs146170087(C;C)
Alt rs146170087(C;C)
Reference rs146170087(T;T)
Significance Pathogenic
Disease Neurodegeneration with brain iron accumulation 4
Variation info
Gene C19orf12
CLNDBN Neurodegeneration with brain iron accumulation 4
Reversed 0
HGVS NC_000019.9:g.30193654T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024154.3,