Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860290(C;T)
Make rs281860290(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219918291
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860290
ebirs281860290
HLIrs281860290
Exacrs281860290
Varsomers281860290
Maprs281860290
PheGenIrs281860290
hapmaprs281860290
1000 genomesrs281860290
hgdprs281860290
ensemblrs281860290
gopubmedrs281860290
geneviewrs281860290
scholarrs281860290
googlers281860290
pharmgkbrs281860290
gwascentralrs281860290
openSNPrs281860290
23andMers281860290
23andMe allrs281860290
SNP Nexus

SNPshotrs281860290
SNPdbers281860290
MSV3drs281860290
GWAS Ctlgrs281860290
Max Magnitude0
ClinVar
Risk rs281860290(T;T)
Alt rs281860290(T;T)
Reference rs281860290(C;C)
Significance Pathogenic
Disease Hypermanganesemia with dystonia
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia, polycythemia and cirrhosis
Reversed 1
HGVS NC_000001.10:g.220091633G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031961.1,