Have questions? Visit https://www.reddit.com/r/SNPedia

rs770519542

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770519542(C;T)
Make rs770519542(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position62630788
GeneGANAB
is asnp
is mentioned by
dbSNPrs770519542
ebirs770519542
HLIrs770519542
Exacrs770519542
Varsomers770519542
Maprs770519542
PheGenIrs770519542
hapmaprs770519542
1000 genomesrs770519542
hgdprs770519542
ensemblrs770519542
gopubmedrs770519542
geneviewrs770519542
scholarrs770519542
googlers770519542
pharmgkbrs770519542
gwascentralrs770519542
openSNPrs770519542
23andMers770519542
23andMe allrs770519542
SNP Nexus

SNPshotrs770519542
SNPdbers770519542
MSV3drs770519542
GWAS Ctlgrs770519542
Max Magnitude0
ClinVar
Risk rs770519542(T;T)
Alt rs770519542(T;T)
Reference rs770519542(C;C)
Significance Pathogenic
Disease Polycystic kidney disease 3
Variation info
Gene GANAB
CLNDBN Polycystic kidney disease 3
Reversed 0
HGVS NC_000011.9:g.62398260C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000239504.1,