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rs727503528

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503528(C;T)
Make rs727503528(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position37769050
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs727503528
ebirs727503528
HLIrs727503528
Exacrs727503528
Varsomers727503528
Maprs727503528
PheGenIrs727503528
hapmaprs727503528
1000 genomesrs727503528
hgdprs727503528
ensemblrs727503528
gopubmedrs727503528
geneviewrs727503528
scholarrs727503528
googlers727503528
pharmgkbrs727503528
gwascentralrs727503528
openSNPrs727503528
23andMers727503528
23andMe allrs727503528
SNP Nexus

SNPshotrs727503528
SNPdbers727503528
MSV3drs727503528
GWAS Ctlgrs727503528
Max Magnitude0
ClinVar
Risk rs727503528(T;T)
Alt rs727503528(T;T)
Reference rs727503528(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TRIOBP
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000022.10:g.38165057C>T
CLNSRC
CLNACC RCV000152152.1,