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rs140511594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140511594(A;A)
Make rs140511594(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position165941111
GeneTTC21B, WNK3
is asnp
is mentioned by
dbSNPrs140511594
ebirs140511594
HLIrs140511594
Exacrs140511594
Varsomers140511594
Maprs140511594
PheGenIrs140511594
hapmaprs140511594
1000 genomesrs140511594
hgdprs140511594
ensemblrs140511594
gopubmedrs140511594
geneviewrs140511594
scholarrs140511594
googlers140511594
pharmgkbrs140511594
gwascentralrs140511594
openSNPrs140511594
23andMers140511594
23andMe allrs140511594
SNP Nexus

SNPshotrs140511594
SNPdbers140511594
MSV3drs140511594
GWAS Ctlgrs140511594
Max Magnitude0
ClinVar
Risk rs140511594(A;A)
Alt rs140511594(A;A)
Reference rs140511594(G;G)
Significance Pathogenic
Disease Nephronophthisis 12
Variation info
Gene TTC21B-AS1 TTC21B
CLNDBN Nephronophthisis 12
Reversed 0
HGVS NC_000002.11:g.166797621G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023924.2,