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rs281860287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860287(-;-)
Make rs281860287(-;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position219927934
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860287
ebirs281860287
HLIrs281860287
Exacrs281860287
Varsomers281860287
Maprs281860287
PheGenIrs281860287
hapmaprs281860287
1000 genomesrs281860287
hgdprs281860287
ensemblrs281860287
gopubmedrs281860287
geneviewrs281860287
scholarrs281860287
googlers281860287
pharmgkbrs281860287
gwascentralrs281860287
openSNPrs281860287
23andMers281860287
23andMe allrs281860287
SNP Nexus

SNPshotrs281860287
SNPdbers281860287
MSV3drs281860287
GWAS Ctlgrs281860287
Max Magnitude0
ClinVar
Risk rs281860287(;)
Alt rs281860287(;)
Reference rs281860287(G;G)
Significance Pathogenic
Disease Hypermanganesemia with dystonia
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia, polycythemia and cirrhosis
Reversed 1
HGVS NC_000001.10:g.220101276delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000023873.4,