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rs773404494

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773404494(G;T)
Make rs773404494(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position53938830
GenePCDH15
is asnp
is mentioned by
dbSNPrs773404494
ebirs773404494
HLIrs773404494
Exacrs773404494
Varsomers773404494
Maprs773404494
PheGenIrs773404494
hapmaprs773404494
1000 genomesrs773404494
hgdprs773404494
ensemblrs773404494
gopubmedrs773404494
geneviewrs773404494
scholarrs773404494
googlers773404494
pharmgkbrs773404494
gwascentralrs773404494
openSNPrs773404494
23andMers773404494
23andMe allrs773404494
SNP Nexus

SNPshotrs773404494
SNPdbers773404494
MSV3drs773404494
GWAS Ctlgrs773404494
Max Magnitude0
ClinVar
Risk rs773404494(T;T)
Alt rs773404494(T;T)
Reference rs773404494(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1F
Reversed 0
HGVS NC_000010.10:g.55698590G>A
CLNSRC
CLNACC RCV000223562.1,