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rs760905589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760905589(A;A)
Make rs760905589(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position84736939
GeneTBX18
is asnp
is mentioned by
dbSNPrs760905589
ebirs760905589
HLIrs760905589
Exacrs760905589
Varsomers760905589
Maprs760905589
PheGenIrs760905589
hapmaprs760905589
1000 genomesrs760905589
hgdprs760905589
ensemblrs760905589
gopubmedrs760905589
geneviewrs760905589
scholarrs760905589
googlers760905589
pharmgkbrs760905589
gwascentralrs760905589
openSNPrs760905589
23andMers760905589
23andMe allrs760905589
SNP Nexus

SNPshotrs760905589
SNPdbers760905589
MSV3drs760905589
GWAS Ctlgrs760905589
Max Magnitude0
ClinVar
Risk rs760905589(A;A)
Alt rs760905589(A;A)
Reference rs760905589(G;G)
Significance Pathogenic
Disease Multicystic renal dysplasia
Variation info
Gene TBX18
CLNDBN Multicystic renal dysplasia, bilateral
Reversed 0
HGVS NC_000006.11:g.85446657G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190535.2,