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rs1064793288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position215782752
GeneUSH2A
is asnp
is mentioned by
dbSNPrs1064793288
dbSNP (old)rs1064793288
ClinGenrs1064793288
ebirs1064793288
HLIrs1064793288
Exacrs1064793288
Gnomadrs1064793288
Varsomers1064793288
Maprs1064793288
PheGenIrs1064793288
Biobankrs1064793288
1000 genomesrs1064793288
hgdprs1064793288
ensemblrs1064793288
gopubmedrs1064793288
geneviewrs1064793288
scholarrs1064793288
googlers1064793288
pharmgkbrs1064793288
gwascentralrs1064793288
openSNPrs1064793288
23andMers1064793288
23andMe allrs1064793288
SNPshotrs1064793288
SNPdbers1064793288
MSV3drs1064793288
GWAS Ctlgrs1064793288
Max Magnitude0
ClinVar
Risk rs1064793288(A;A)
Alt rs1064793288(A;A)
Reference Rs1064793288(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.215956094G>T
CLNSRC
CLNACC RCV000478468.1,