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rs766132877

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs766132877(C;C)
Make rs766132877(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165899882
GeneTTC21B
is asnp
is mentioned by
dbSNPrs766132877
ebirs766132877
HLIrs766132877
Exacrs766132877
Varsomers766132877
Maprs766132877
PheGenIrs766132877
hapmaprs766132877
1000 genomesrs766132877
hgdprs766132877
ensemblrs766132877
gopubmedrs766132877
geneviewrs766132877
scholarrs766132877
googlers766132877
pharmgkbrs766132877
gwascentralrs766132877
openSNPrs766132877
23andMers766132877
23andMe allrs766132877
SNP Nexus

SNPshotrs766132877
SNPdbers766132877
MSV3drs766132877
GWAS Ctlgrs766132877
Max Magnitude0
ClinVar
Risk rs766132877(C;C)
Alt rs766132877(C;C)
Reference rs766132877(T;T)
Significance Pathogenic
Disease Nephronophthisis 12
Variation info
Gene TTC21B
CLNDBN Nephronophthisis 12
Reversed 0
HGVS NC_000002.11:g.166756392T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023926.3,