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rs397517429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517429(-;-)
Make rs397517429(-;A)
Make rs397517429(A;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position90644841
GeneGPR98
is asnp
is mentioned by
dbSNPrs397517429
ebirs397517429
HLIrs397517429
Exacrs397517429
Varsomers397517429
Maprs397517429
PheGenIrs397517429
hapmaprs397517429
1000 genomesrs397517429
hgdprs397517429
ensemblrs397517429
gopubmedrs397517429
geneviewrs397517429
scholarrs397517429
googlers397517429
pharmgkbrs397517429
gwascentralrs397517429
openSNPrs397517429
23andMers397517429
23andMe allrs397517429
SNP Nexus

SNPshotrs397517429
SNPdbers397517429
MSV3drs397517429
GWAS Ctlgrs397517429
Max Magnitude0
ClinVar
Risk rs397517429(A;A)
Alt rs397517429(A;A)
Reference rs397517429(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89940658dupA
CLNSRC ClinVar
CLNACC RCV000039565.2,