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rs387907173

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907173(A;A)
Make rs387907173(A;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position29702776
GeneC19orf12
is asnp
is mentioned by
dbSNPrs387907173
ebirs387907173
HLIrs387907173
Exacrs387907173
Varsomers387907173
Maprs387907173
PheGenIrs387907173
hapmaprs387907173
1000 genomesrs387907173
hgdprs387907173
ensemblrs387907173
gopubmedrs387907173
geneviewrs387907173
scholarrs387907173
googlers387907173
pharmgkbrs387907173
gwascentralrs387907173
openSNPrs387907173
23andMers387907173
23andMe allrs387907173
SNP Nexus

SNPshotrs387907173
SNPdbers387907173
MSV3drs387907173
GWAS Ctlgrs387907173
Max Magnitude0
ClinVar
Risk rs387907173(A;A)
Alt rs387907173(A;A)
Reference rs387907173(T;T)
Significance Pathogenic
Disease Neurodegeneration with brain iron accumulation 4
Variation info
Gene C19orf12
CLNDBN Neurodegeneration with brain iron accumulation 4
Reversed 1
HGVS NC_000019.9:g.30193683A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024323.3,