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rs797045022

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045022(A;G)
Make rs797045022(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position84762554
GeneTBX18
is asnp
is mentioned by
dbSNPrs797045022
ebirs797045022
HLIrs797045022
Exacrs797045022
Varsomers797045022
Maprs797045022
PheGenIrs797045022
hapmaprs797045022
1000 genomesrs797045022
hgdprs797045022
ensemblrs797045022
gopubmedrs797045022
geneviewrs797045022
scholarrs797045022
googlers797045022
pharmgkbrs797045022
gwascentralrs797045022
openSNPrs797045022
23andMers797045022
23andMe allrs797045022
SNP Nexus

SNPshotrs797045022
SNPdbers797045022
MSV3drs797045022
GWAS Ctlgrs797045022
Max Magnitude0
ClinVar
Risk rs797045022(G;G)
Alt rs797045022(G;G)
Reference rs797045022(A;A)
Significance Pathogenic
Disease Multicystic renal dysplasia
Variation info
Gene TBX18
CLNDBN Multicystic renal dysplasia, bilateral
Reversed 1
HGVS NC_000006.11:g.85472272T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190536.2,