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rs727504777

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504777(C;T)
Make rs727504777(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position90778008
GeneADGRV1
is asnp
is mentioned by
dbSNPrs727504777
ebirs727504777
HLIrs727504777
Exacrs727504777
Varsomers727504777
Maprs727504777
PheGenIrs727504777
hapmaprs727504777
1000 genomesrs727504777
hgdprs727504777
ensemblrs727504777
gopubmedrs727504777
geneviewrs727504777
scholarrs727504777
googlers727504777
pharmgkbrs727504777
gwascentralrs727504777
openSNPrs727504777
23andMers727504777
23andMe allrs727504777
SNP Nexus

SNPshotrs727504777
SNPdbers727504777
MSV3drs727504777
GWAS Ctlgrs727504777
Max Magnitude0
ClinVar
Risk rs727504777(T;T)
Alt rs727504777(T;T)
Reference rs727504777(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90073825C>T
CLNSRC
CLNACC RCV000156094.1,