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rs281860288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860288(-;-)
Make rs281860288(-;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position219927856
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860288
ebirs281860288
HLIrs281860288
Exacrs281860288
Varsomers281860288
Maprs281860288
PheGenIrs281860288
hapmaprs281860288
1000 genomesrs281860288
hgdprs281860288
ensemblrs281860288
gopubmedrs281860288
geneviewrs281860288
scholarrs281860288
googlers281860288
pharmgkbrs281860288
gwascentralrs281860288
openSNPrs281860288
23andMers281860288
23andMe allrs281860288
SNP Nexus

SNPshotrs281860288
SNPdbers281860288
MSV3drs281860288
GWAS Ctlgrs281860288
Max Magnitude0
ClinVar
Risk rs281860288(;)
Alt rs281860288(;)
Reference rs281860288(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.220101198delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000023872.4,