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rs267607067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607067(-;-)
Make rs267607067(-;A)
ReferenceGRCh38 38.1/141
Chromosome16
Position31486201
GeneSLC5A2
is asnp
is mentioned by
dbSNPrs267607067
ebirs267607067
HLIrs267607067
Exacrs267607067
Varsomers267607067
Maprs267607067
PheGenIrs267607067
hapmaprs267607067
1000 genomesrs267607067
hgdprs267607067
ensemblrs267607067
gopubmedrs267607067
geneviewrs267607067
scholarrs267607067
googlers267607067
pharmgkbrs267607067
gwascentralrs267607067
openSNPrs267607067
23andMers267607067
23andMe allrs267607067
SNP Nexus

SNPshotrs267607067
SNPdbers267607067
MSV3drs267607067
GWAS Ctlgrs267607067
Max Magnitude0
ClinVar
Risk rs267607067(;)
Alt rs267607067(;)
Reference rs267607067(A;A)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.9:g.31497522delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000013769.19,