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rs371981035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs371981035(A;G)
Make rs371981035(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position90810231
GeneGPR98
is asnp
is mentioned by
dbSNPrs371981035
ebirs371981035
HLIrs371981035
Exacrs371981035
Varsomers371981035
Maprs371981035
PheGenIrs371981035
hapmaprs371981035
1000 genomesrs371981035
hgdprs371981035
ensemblrs371981035
gopubmedrs371981035
geneviewrs371981035
scholarrs371981035
googlers371981035
pharmgkbrs371981035
gwascentralrs371981035
openSNPrs371981035
23andMers371981035
23andMe allrs371981035
SNP Nexus

SNPshotrs371981035
SNPdbers371981035
MSV3drs371981035
GWAS Ctlgrs371981035
Max Magnitude0
ClinVar
Risk rs371981035(G;G)
Alt rs371981035(G;G)
Reference rs371981035(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene ADGRV1 GPR98
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90106048A>G
CLNSRC ClinVar
CLNACC RCV000039531.2,