Have questions? Visit https://www.reddit.com/r/SNPedia

rs527236131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236131(C;T)
Make rs527236131(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position90810996
GeneGPR98
is asnp
is mentioned by
dbSNPrs527236131
ebirs527236131
HLIrs527236131
Exacrs527236131
Varsomers527236131
Maprs527236131
PheGenIrs527236131
hapmaprs527236131
1000 genomesrs527236131
hgdprs527236131
ensemblrs527236131
gopubmedrs527236131
geneviewrs527236131
scholarrs527236131
googlers527236131
pharmgkbrs527236131
gwascentralrs527236131
openSNPrs527236131
23andMers527236131
23andMe allrs527236131
SNP Nexus

SNPshotrs527236131
SNPdbers527236131
MSV3drs527236131
GWAS Ctlgrs527236131
Max Magnitude0
ClinVar
Risk rs527236131(T;T)
Alt rs527236131(T;T)
Reference rs527236131(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90106813C>T
CLNSRC ClinVar
CLNACC RCV000132686.1,