Have questions? Visit https://www.reddit.com/r/SNPedia

rs886043626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position74919525
GeneUSH1G
is asnp
is mentioned by
dbSNPrs886043626
dbSNP (classic)rs886043626
ClinGenrs886043626
ebirs886043626
HLIrs886043626
Exacrs886043626
Gnomadrs886043626
Varsomers886043626
LitVarrs886043626
Maprs886043626
PheGenIrs886043626
Biobankrs886043626
1000 genomesrs886043626
hgdprs886043626
ensemblrs886043626
geneviewrs886043626
scholarrs886043626
googlers886043626
pharmgkbrs886043626
gwascentralrs886043626
openSNPrs886043626
23andMers886043626
23andMe allrs886043626
SNPshotrs886043626
SNPdbers886043626
MSV3drs886043626
GWAS Ctlgrs886043626
Max Magnitude0
ClinVar
Risk rs886043626(-;-)
Alt rs886043626(-;-)
Reference Rs886043626(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH1G
CLNDBN Usher syndrome, type 1G
Reversed 0
HGVS NC_000017.10:g.72915620delC
CLNSRC
CLNACC RCV000333423.1,