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rs527236132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236132(G;T)
Make rs527236132(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position90774304
GeneGPR98
is asnp
is mentioned by
dbSNPrs527236132
ebirs527236132
HLIrs527236132
Exacrs527236132
Varsomers527236132
Maprs527236132
PheGenIrs527236132
hapmaprs527236132
1000 genomesrs527236132
hgdprs527236132
ensemblrs527236132
gopubmedrs527236132
geneviewrs527236132
scholarrs527236132
googlers527236132
pharmgkbrs527236132
gwascentralrs527236132
openSNPrs527236132
23andMers527236132
23andMe allrs527236132
SNP Nexus

SNPshotrs527236132
SNPdbers527236132
MSV3drs527236132
GWAS Ctlgrs527236132
Max Magnitude0
ClinVar
Risk rs527236132(T;T)
Alt rs527236132(T;T)
Reference Rs527236132(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90070121G>T
CLNSRC ClinVar
CLNACC RCV000132685.1,