rs587776926

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs587776926(C;C)

Make rs587776926(C;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

26045107

Gene

SLC30A2

is a	snp
is	mentioned by
dbSNP	rs587776926
dbSNP (classic)	rs587776926
ClinGen	rs587776926
ebi	rs587776926
HLI	rs587776926
Exac	rs587776926
Gnomad	rs587776926
Varsome	rs587776926
LitVar	rs587776926
Map	rs587776926
PheGenI	rs587776926
Biobank	rs587776926
1000 genomes	rs587776926
hgdp	rs587776926
ensembl	rs587776926
geneview	rs587776926
scholar	rs587776926
google	rs587776926
pharmgkb	rs587776926
gwascentral	rs587776926
openSNP	rs587776926
23andMe	rs587776926
SNPshot	rs587776926
SNPdbe	rs587776926
MSV3d	rs587776926
GWAS Ctlg	rs587776926

Max Magnitude

0

ClinVar
Risk	rs587776926(C;C) Rs587776926(T;T)
Alt	rs587776926(C;C) Rs587776926(T;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 UniProtKB (protein)
CLNACC	RCV000032750.3,