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rs876657647

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657647(G;G)
Make rs876657647(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position90759569
GeneADGRV1
is asnp
is mentioned by
dbSNPrs876657647
ebirs876657647
HLIrs876657647
Exacrs876657647
Varsomers876657647
Maprs876657647
PheGenIrs876657647
hapmaprs876657647
1000 genomesrs876657647
hgdprs876657647
ensemblrs876657647
gopubmedrs876657647
geneviewrs876657647
scholarrs876657647
googlers876657647
pharmgkbrs876657647
gwascentralrs876657647
openSNPrs876657647
23andMers876657647
23andMe allrs876657647
SNP Nexus

SNPshotrs876657647
SNPdbers876657647
MSV3drs876657647
GWAS Ctlgrs876657647
Max Magnitude0
ClinVar
Risk rs876657647(G;G)
Alt rs876657647(G;G)
Reference rs876657647(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90055386T>G
CLNSRC
CLNACC RCV000221151.1,