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rs281860291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860291(C;C)
Make rs281860291(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219915861
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860291
ebirs281860291
HLIrs281860291
Exacrs281860291
Varsomers281860291
Maprs281860291
PheGenIrs281860291
hapmaprs281860291
1000 genomesrs281860291
hgdprs281860291
ensemblrs281860291
gopubmedrs281860291
geneviewrs281860291
scholarrs281860291
googlers281860291
pharmgkbrs281860291
gwascentralrs281860291
openSNPrs281860291
23andMers281860291
23andMe allrs281860291
SNP Nexus

SNPshotrs281860291
SNPdbers281860291
MSV3drs281860291
GWAS Ctlgrs281860291
Max Magnitude0
ClinVar
Risk rs281860291(C;C)
Alt rs281860291(C;C)
Reference rs281860291(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.220089203A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031957.1,