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rs1057519590

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519590(-;-)
Make rs1057519590(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position219927949
GeneLOC107985281, SLC30A10
is asnp
is mentioned by
dbSNPrs1057519590
dbSNP (old)rs1057519590
ClinGenrs1057519590
ebirs1057519590
HLIrs1057519590
Exacrs1057519590
Gnomadrs1057519590
Varsomers1057519590
Maprs1057519590
PheGenIrs1057519590
Biobankrs1057519590
1000 genomesrs1057519590
hgdprs1057519590
ensemblrs1057519590
gopubmedrs1057519590
geneviewrs1057519590
scholarrs1057519590
googlers1057519590
pharmgkbrs1057519590
gwascentralrs1057519590
openSNPrs1057519590
23andMers1057519590
23andMe allrs1057519590
SNPshotrs1057519590
SNPdbers1057519590
MSV3drs1057519590
GWAS Ctlgrs1057519590
Max Magnitude0
ClinVar
Risk rs1057519590(-;-)
Alt rs1057519590(-;-)
Reference Rs1057519590(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.220101291delG
CLNSRC
CLNACC RCV000417082.1,