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rs281860289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGT;GGT) 0 common in clinvar
Make rs281860289(-;-)
Make rs281860289(-;GGT)
ReferenceGRCh38 38.1/141
Chromosome1
Position219918446
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860289
ebirs281860289
HLIrs281860289
Exacrs281860289
Varsomers281860289
Maprs281860289
PheGenIrs281860289
hapmaprs281860289
1000 genomesrs281860289
hgdprs281860289
ensemblrs281860289
gopubmedrs281860289
geneviewrs281860289
scholarrs281860289
googlers281860289
pharmgkbrs281860289
gwascentralrs281860289
openSNPrs281860289
23andMers281860289
23andMe allrs281860289
SNP Nexus

SNPshotrs281860289
SNPdbers281860289
MSV3drs281860289
GWAS Ctlgrs281860289
Max Magnitude0
ClinVar
Risk rs281860289(;)
Alt rs281860289(;)
Reference rs281860289(GGT;GGT)
Significance Pathogenic
Disease Hypermanganesemia with dystonia
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia, polycythemia and cirrhosis
Reversed 1
HGVS NC_000001.10:g.220091788_220091790delACC
CLNSRC ClinVar GeneReviews
CLNACC RCV000031960.1,