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rs1064795047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position215889056
GeneUSH2A
is asnp
is mentioned by
dbSNPrs1064795047
dbSNP (classic)rs1064795047
ClinGenrs1064795047
ebirs1064795047
HLIrs1064795047
Exacrs1064795047
Gnomadrs1064795047
Varsomers1064795047
LitVarrs1064795047
Maprs1064795047
PheGenIrs1064795047
Biobankrs1064795047
1000 genomesrs1064795047
hgdprs1064795047
ensemblrs1064795047
geneviewrs1064795047
scholarrs1064795047
googlers1064795047
pharmgkbrs1064795047
gwascentralrs1064795047
openSNPrs1064795047
23andMers1064795047
SNPshotrs1064795047
SNPdbers1064795047
MSV3drs1064795047
GWAS Ctlgrs1064795047
Max Magnitude0
ClinVar
Risk rs1064795047(G;G)
Alt rs1064795047(G;G)
Reference Rs1064795047(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216062398T>C
CLNSRC
CLNACC RCV000486199.1,