rs387906682

Orientation

plus

Stabilized

plus

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

Make rs387906682(C;G)

Make rs387906682(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31489034

Gene	C16orf58, SLC5A2

is a	snp
is	mentioned by
dbSNP	rs387906682
dbSNP (classic)	rs387906682
ClinGen	rs387906682
ebi	rs387906682
HLI	rs387906682
Exac	rs387906682
Gnomad	rs387906682
Varsome	rs387906682
LitVar	rs387906682
Map	rs387906682
PheGenI	rs387906682
Biobank	rs387906682
1000 genomes	rs387906682
hgdp	rs387906682
ensembl	rs387906682
geneview	rs387906682
scholar	rs387906682
google	rs387906682
pharmgkb	rs387906682
gwascentral	rs387906682
openSNP	rs387906682
23andMe	rs387906682
SNPshot	rs387906682
SNPdbe	rs387906682
MSV3d	rs387906682
GWAS Ctlg	rs387906682

Max Magnitude

0

ClinVar
Risk	rs387906682(G;G)
Alt	rs387906682(G;G)
Reference	Rs387906682(C;C)
Significance	Pathogenic
Disease	Familial renal glucosuria
Variation	info
Gene	SLC5A2 C16orf58
CLNDBN	Familial renal glucosuria
Reversed	0
HGVS	NC_000016.9:g.31500355C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000408654.1,