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

rs879253766

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253766(A;A)
Make rs879253766(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position22416280
GeneSLC39A14
is asnp
is mentioned by
dbSNPrs879253766
ebirs879253766
HLIrs879253766
Exacrs879253766
Varsomers879253766
Maprs879253766
PheGenIrs879253766
hapmaprs879253766
1000 genomesrs879253766
hgdprs879253766
ensemblrs879253766
gopubmedrs879253766
geneviewrs879253766
scholarrs879253766
googlers879253766
pharmgkbrs879253766
gwascentralrs879253766
openSNPrs879253766
23andMers879253766
23andMe allrs879253766
SNP Nexus

SNPshotrs879253766
SNPdbers879253766
MSV3drs879253766
GWAS Ctlgrs879253766
Max Magnitude0
ClinVar
Risk rs879253766(A;A)
Alt rs879253766(A;A)
Reference rs879253766(G;G)
Significance Pathogenic
Disease Hypermanganesemia with dystonia 2
Variation info
Gene SLC39A14
CLNDBN Hypermanganesemia with dystonia 2
Reversed 0
HGVS NC_000008.10:g.22273793G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234927.1,