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rs149925563

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs149925563(A;A)
Make rs149925563(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165941046
GeneTTC21B, TTC21B-AS1
is asnp
is mentioned by
dbSNPrs149925563
ebirs149925563
HLIrs149925563
Exacrs149925563
Varsomers149925563
Maprs149925563
PheGenIrs149925563
hapmaprs149925563
1000 genomesrs149925563
hgdprs149925563
ensemblrs149925563
gopubmedrs149925563
geneviewrs149925563
scholarrs149925563
googlers149925563
pharmgkbrs149925563
gwascentralrs149925563
openSNPrs149925563
23andMers149925563
23andMe allrs149925563
SNP Nexus

SNPshotrs149925563
SNPdbers149925563
MSV3drs149925563
GWAS Ctlgrs149925563
Max Magnitude0
ClinVar
Risk rs149925563(A;A)
Alt rs149925563(A;A)
Reference rs149925563(T;T)
Significance Pathogenic
Disease not provided Nephronophthisis 12
Variation info
Gene TTC21B-AS1 TTC21B
CLNDBN not provided Nephronophthisis 12
Reversed 0
HGVS NC_000002.11:g.166797556T>A
CLNSRC
CLNACC RCV000179530.1, RCV000195266.1,