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rs281860284

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860284(C;C)
Make rs281860284(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219928175
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860284
ebirs281860284
HLIrs281860284
Exacrs281860284
Varsomers281860284
Maprs281860284
PheGenIrs281860284
hapmaprs281860284
1000 genomesrs281860284
hgdprs281860284
ensemblrs281860284
gopubmedrs281860284
geneviewrs281860284
scholarrs281860284
googlers281860284
pharmgkbrs281860284
gwascentralrs281860284
openSNPrs281860284
23andMers281860284
23andMe allrs281860284
SNP Nexus

SNPshotrs281860284
SNPdbers281860284
MSV3drs281860284
GWAS Ctlgrs281860284
Max Magnitude0
ClinVar
Risk rs281860284(C;C)
Alt rs281860284(C;C)
Reference rs281860284(T;T)
Significance Pathogenic
Disease Hypermanganesemia with dystonia
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia, polycythemia and cirrhosis
Reversed 1
HGVS NC_000001.10:g.220101517A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023871.4,