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rs398122802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122802(A;A)
Make rs398122802(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position31484914
GeneSLC5A2
is asnp
is mentioned by
dbSNPrs398122802
ebirs398122802
HLIrs398122802
Exacrs398122802
Varsomers398122802
Maprs398122802
PheGenIrs398122802
hapmaprs398122802
1000 genomesrs398122802
hgdprs398122802
ensemblrs398122802
gopubmedrs398122802
geneviewrs398122802
scholarrs398122802
googlers398122802
pharmgkbrs398122802
gwascentralrs398122802
openSNPrs398122802
23andMers398122802
23andMe allrs398122802
SNP Nexus

SNPshotrs398122802
SNPdbers398122802
MSV3drs398122802
GWAS Ctlgrs398122802
Max Magnitude0
ClinVar
Risk rs398122802(A;A)
Alt rs398122802(A;A)
Reference rs398122802(C;C)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.9:g.31496235C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022763.24,