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rs397517426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517426(-;-)
Make rs397517426(-;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position90855808
GeneGPR98
is asnp
is mentioned by
dbSNPrs397517426
ebirs397517426
HLIrs397517426
Exacrs397517426
Varsomers397517426
Maprs397517426
PheGenIrs397517426
hapmaprs397517426
1000 genomesrs397517426
hgdprs397517426
ensemblrs397517426
gopubmedrs397517426
geneviewrs397517426
scholarrs397517426
googlers397517426
pharmgkbrs397517426
gwascentralrs397517426
openSNPrs397517426
23andMers397517426
23andMe allrs397517426
SNP Nexus

SNPshotrs397517426
SNPdbers397517426
MSV3drs397517426
GWAS Ctlgrs397517426
Max Magnitude0
ClinVar
Risk rs397517426(;)
Alt rs397517426(;)
Reference rs397517426(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90151625delT
CLNSRC ClinVar
CLNACC RCV000039548.2,