rs1057521634

Orientation

minus

Stabilized

minus

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

Make rs1057521634(C;C)

Make rs1057521634(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

84017180

Gene

SLC38A8

is a	snp
is	mentioned by
dbSNP	rs1057521634
dbSNP (classic)	rs1057521634
ClinGen	rs1057521634
ebi	rs1057521634
HLI	rs1057521634
Exac	rs1057521634
Gnomad	rs1057521634
Varsome	rs1057521634
LitVar	rs1057521634
Map	rs1057521634
PheGenI	rs1057521634
Biobank	rs1057521634
1000 genomes	rs1057521634
hgdp	rs1057521634
ensembl	rs1057521634
geneview	rs1057521634
scholar	rs1057521634
google	rs1057521634
pharmgkb	rs1057521634
gwascentral	rs1057521634
openSNP	rs1057521634
23andMe	rs1057521634
SNPshot	rs1057521634
SNPdbe	rs1057521634
MSV3d	rs1057521634
GWAS Ctlg	rs1057521634

Max Magnitude

0

ClinVar
Risk	rs1057521634(C;C)
Alt	rs1057521634(C;C)
Reference	Rs1057521634(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SLC38A8
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.84050785A>G
CLNSRC
CLNACC	RCV000429596.1,