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rs387906682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906682(C;G)
Make rs387906682(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31489034
GeneC16orf58, SLC5A2
is asnp
is mentioned by
dbSNPrs387906682
ebirs387906682
HLIrs387906682
Exacrs387906682
Varsomers387906682
Maprs387906682
PheGenIrs387906682
hapmaprs387906682
1000 genomesrs387906682
hgdprs387906682
ensemblrs387906682
gopubmedrs387906682
geneviewrs387906682
scholarrs387906682
googlers387906682
pharmgkbrs387906682
gwascentralrs387906682
openSNPrs387906682
23andMers387906682
23andMe allrs387906682
SNP Nexus

SNPshotrs387906682
SNPdbers387906682
MSV3drs387906682
GWAS Ctlgrs387906682
Max Magnitude0
ClinVar
Risk rs387906682(G;G)
Alt rs387906682(G;G)
Reference rs387906682(C;C)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene C16orf58 SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.9:g.31500355C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022761.25,