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rs1060499796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499796(A;A)
Make rs1060499796(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position90644869
GeneADGRV1
is asnp
is mentioned by
dbSNPrs1060499796
dbSNP (classic)rs1060499796
ClinGenrs1060499796
ebirs1060499796
HLIrs1060499796
Exacrs1060499796
Gnomadrs1060499796
Varsomers1060499796
LitVarrs1060499796
Maprs1060499796
PheGenIrs1060499796
Biobankrs1060499796
1000 genomesrs1060499796
hgdprs1060499796
ensemblrs1060499796
geneviewrs1060499796
scholarrs1060499796
googlers1060499796
pharmgkbrs1060499796
gwascentralrs1060499796
openSNPrs1060499796
23andMers1060499796
23andMe allrs1060499796
SNPshotrs1060499796
SNPdbers1060499796
MSV3drs1060499796
GWAS Ctlgrs1060499796
Max Magnitude0
ClinVar
Risk rs1060499796(A;A)
Alt rs1060499796(A;A)
Reference Rs1060499796(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene ADGRV1 GPR98
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89940686G>A
CLNSRC
CLNACC RCV000454318.1,