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rs41308425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41308425(C;G)
Make rs41308425(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position215837990
GeneUSH2A
is asnp
is mentioned by
dbSNPrs41308425
ebirs41308425
HLIrs41308425
Exacrs41308425
Varsomers41308425
Maprs41308425
PheGenIrs41308425
hapmaprs41308425
1000 genomesrs41308425
hgdprs41308425
ensemblrs41308425
gopubmedrs41308425
geneviewrs41308425
scholarrs41308425
googlers41308425
pharmgkbrs41308425
gwascentralrs41308425
openSNPrs41308425
23andMers41308425
23andMe allrs41308425
SNP Nexus

SNPshotrs41308425
SNPdbers41308425
MSV3drs41308425
GWAS Ctlgrs41308425
Max Magnitude0
ClinVar
Risk rs41308425(G;G)
Alt rs41308425(G;G)
Reference rs41308425(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 0
HGVS NC_000001.10:g.216011332C>G
CLNSRC ClinVar
CLNACC RCV000041950.2,