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rs201987973

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201987973(A;A)
Make rs201987973(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position29702923
GeneC19orf12
is asnp
is mentioned by
dbSNPrs201987973
ebirs201987973
HLIrs201987973
Exacrs201987973
Varsomers201987973
Maprs201987973
PheGenIrs201987973
hapmaprs201987973
1000 genomesrs201987973
hgdprs201987973
ensemblrs201987973
gopubmedrs201987973
geneviewrs201987973
scholarrs201987973
googlers201987973
pharmgkbrs201987973
gwascentralrs201987973
openSNPrs201987973
23andMers201987973
23andMe allrs201987973
SNP Nexus

SNPshotrs201987973
SNPdbers201987973
MSV3drs201987973
GWAS Ctlgrs201987973
Max Magnitude0
ClinVar
Risk rs201987973(A;A)
Alt rs201987973(A;A)
Reference rs201987973(G;G)
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.30193830G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211114.1,