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rs387907059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907059(A;A)
Make rs387907059(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position165919294
GeneTTC21B
is asnp
is mentioned by
dbSNPrs387907059
ebirs387907059
HLIrs387907059
Exacrs387907059
Varsomers387907059
Maprs387907059
PheGenIrs387907059
hapmaprs387907059
1000 genomesrs387907059
hgdprs387907059
ensemblrs387907059
gopubmedrs387907059
geneviewrs387907059
scholarrs387907059
googlers387907059
pharmgkbrs387907059
gwascentralrs387907059
openSNPrs387907059
23andMers387907059
23andMe allrs387907059
SNP Nexus

SNPshotrs387907059
SNPdbers387907059
MSV3drs387907059
GWAS Ctlgrs387907059
Max Magnitude0
ClinVar
Risk rs387907059(A;A)
Alt rs387907059(A;A)
Reference rs387907059(T;T)
Significance Pathogenic
Disease Nephronophthisis 12
Variation info
Gene TTC21B
CLNDBN Nephronophthisis 12
Reversed 1
HGVS NC_000002.11:g.166775804A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023925.3,