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rs886037850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037850(A;A)
Make rs886037850(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position31484885
GeneSLC5A2
is asnp
is mentioned by
dbSNPrs886037850
dbSNP (classic)rs886037850
ClinGenrs886037850
ebirs886037850
HLIrs886037850
Exacrs886037850
Gnomadrs886037850
Varsomers886037850
LitVarrs886037850
Maprs886037850
PheGenIrs886037850
Biobankrs886037850
1000 genomesrs886037850
hgdprs886037850
ensemblrs886037850
geneviewrs886037850
scholarrs886037850
googlers886037850
pharmgkbrs886037850
gwascentralrs886037850
openSNPrs886037850
23andMers886037850
SNPshotrs886037850
SNPdbers886037850
MSV3drs886037850
GWAS Ctlgrs886037850
Max Magnitude0
ClinVar
Risk rs886037850(A;A)
Alt rs886037850(A;A)
Reference Rs886037850(G;G)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.9:g.31496206G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000239563.1,