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rs281860292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860292(-;-)
Make rs281860292(-;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position219915672
GeneSLC30A10
is asnp
is mentioned by
dbSNPrs281860292
ebirs281860292
HLIrs281860292
Exacrs281860292
Varsomers281860292
Maprs281860292
PheGenIrs281860292
hapmaprs281860292
1000 genomesrs281860292
hgdprs281860292
ensemblrs281860292
gopubmedrs281860292
geneviewrs281860292
scholarrs281860292
googlers281860292
pharmgkbrs281860292
gwascentralrs281860292
openSNPrs281860292
23andMers281860292
23andMe allrs281860292
SNP Nexus

SNPshotrs281860292
SNPdbers281860292
MSV3drs281860292
GWAS Ctlgrs281860292
Max Magnitude0
ClinVar
Risk rs281860292(;)
Alt rs281860292(;)
Reference rs281860292(A;A)
Significance Pathogenic
Disease Hypermanganesemia with dystonia
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia, polycythemia and cirrhosis
Reversed 1
HGVS NC_000001.10:g.220089014delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000023874.4,