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rs1057519589

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519589(C;T)
Make rs1057519589(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position219927981
GeneLOC107985281, SLC30A10
is asnp
is mentioned by
dbSNPrs1057519589
dbSNP (old)rs1057519589
ClinGenrs1057519589
ebirs1057519589
HLIrs1057519589
Exacrs1057519589
Gnomadrs1057519589
Varsomers1057519589
Maprs1057519589
PheGenIrs1057519589
Biobankrs1057519589
1000 genomesrs1057519589
hgdprs1057519589
ensemblrs1057519589
gopubmedrs1057519589
geneviewrs1057519589
scholarrs1057519589
googlers1057519589
pharmgkbrs1057519589
gwascentralrs1057519589
openSNPrs1057519589
23andMers1057519589
23andMe allrs1057519589
SNPshotrs1057519589
SNPdbers1057519589
MSV3drs1057519589
GWAS Ctlgrs1057519589
Max Magnitude0
ClinVar
Risk rs1057519589(T;T)
Alt rs1057519589(T;T)
Reference Rs1057519589(C;C)
Significance Pathogenic
Disease Hypermanganesemia with dystonia 1
Variation info
Gene SLC30A10
CLNDBN Hypermanganesemia with dystonia 1
Reversed 1
HGVS NC_000001.10:g.220101323G>A
CLNSRC
CLNACC RCV000417078.1,