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rs397517441

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517441(-;-)
Make rs397517441(-;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position90708822
GeneGPR98
is asnp
is mentioned by
dbSNPrs397517441
ebirs397517441
HLIrs397517441
Exacrs397517441
Varsomers397517441
Maprs397517441
PheGenIrs397517441
hapmaprs397517441
1000 genomesrs397517441
hgdprs397517441
ensemblrs397517441
gopubmedrs397517441
geneviewrs397517441
scholarrs397517441
googlers397517441
pharmgkbrs397517441
gwascentralrs397517441
openSNPrs397517441
23andMers397517441
23andMe allrs397517441
SNP Nexus

SNPshotrs397517441
SNPdbers397517441
MSV3drs397517441
GWAS Ctlgrs397517441
Max Magnitude0
ClinVar
Risk rs397517441(;)
Alt rs397517441(;)
Reference rs397517441(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90004639delG
CLNSRC ClinVar
CLNACC RCV000039655.2,