rs281860291

Orientation

minus

Stabilized

minus

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

Make rs281860291(C;C)

Make rs281860291(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

219915861

Gene

SLC30A10

is a	snp
is	mentioned by
dbSNP	rs281860291
dbSNP (classic)	rs281860291
ClinGen	rs281860291
ebi	rs281860291
HLI	rs281860291
Exac	rs281860291
Gnomad	rs281860291
Varsome	rs281860291
LitVar	rs281860291
Map	rs281860291
PheGenI	rs281860291
Biobank	rs281860291
1000 genomes	rs281860291
hgdp	rs281860291
ensembl	rs281860291
geneview	rs281860291
scholar	rs281860291
google	rs281860291
pharmgkb	rs281860291
gwascentral	rs281860291
openSNP	rs281860291
23andMe	rs281860291
SNPshot	rs281860291
SNPdbe	rs281860291
MSV3d	rs281860291
GWAS Ctlg	rs281860291

Max Magnitude

0

ClinVar
Risk	rs281860291(C;C)
Alt	rs281860291(C;C)
Reference	Rs281860291(T;T)
Significance	Pathogenic
Disease	Hypermanganesemia with dystonia 1
Variation	info
Gene	SLC30A10
CLNDBN	Hypermanganesemia with dystonia 1
Reversed	1
HGVS	NC_000001.10:g.220089203A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000031957.1,