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rs727503076

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503076(-;-)
Make rs727503076(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position90681433
GeneADGRV1
is asnp
is mentioned by
dbSNPrs727503076
ebirs727503076
HLIrs727503076
Exacrs727503076
Varsomers727503076
Maprs727503076
PheGenIrs727503076
hapmaprs727503076
1000 genomesrs727503076
hgdprs727503076
ensemblrs727503076
gopubmedrs727503076
geneviewrs727503076
scholarrs727503076
googlers727503076
pharmgkbrs727503076
gwascentralrs727503076
openSNPrs727503076
23andMers727503076
23andMe allrs727503076
SNP Nexus

SNPshotrs727503076
SNPdbers727503076
MSV3drs727503076
GWAS Ctlgrs727503076
Max Magnitude0
ClinVar
Risk rs727503076(;)
Alt rs727503076(;)
Reference rs727503076(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89977250delG
CLNSRC
CLNACC RCV000150761.1,