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rs587776926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776926(C;C)
Make rs587776926(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position26045107
GeneSLC30A2
is asnp
is mentioned by
dbSNPrs587776926
ebirs587776926
HLIrs587776926
Exacrs587776926
Varsomers587776926
Maprs587776926
PheGenIrs587776926
hapmaprs587776926
1000 genomesrs587776926
hgdprs587776926
ensemblrs587776926
gopubmedrs587776926
geneviewrs587776926
scholarrs587776926
googlers587776926
pharmgkbrs587776926
gwascentralrs587776926
openSNPrs587776926
23andMers587776926
23andMe allrs587776926
SNP Nexus

SNPshotrs587776926
SNPdbers587776926
MSV3drs587776926
GWAS Ctlgrs587776926
Max Magnitude0
ClinVar
Risk rs587776926(C,T;C,T)
Alt rs587776926(C,T;C,T)
Reference rs587776926(A;A)
Significance Pathogenic
Disease Zinc deficiency
Variation info
Gene LOC101928681 SLC30A2
CLNDBN Zinc deficiency, transient neonatal
Reversed 1
HGVS NC_000001.10:g.26371598T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000032750.2,