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rs1064797134

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position215878800
GeneUSH2A
is asnp
is mentioned by
dbSNPrs1064797134
dbSNP (old)rs1064797134
ClinGenrs1064797134
ebirs1064797134
HLIrs1064797134
Exacrs1064797134
Gnomadrs1064797134
Varsomers1064797134
Maprs1064797134
PheGenIrs1064797134
Biobankrs1064797134
1000 genomesrs1064797134
hgdprs1064797134
ensemblrs1064797134
gopubmedrs1064797134
geneviewrs1064797134
scholarrs1064797134
googlers1064797134
pharmgkbrs1064797134
gwascentralrs1064797134
openSNPrs1064797134
23andMers1064797134
23andMe allrs1064797134
SNPshotrs1064797134
SNPdbers1064797134
MSV3drs1064797134
GWAS Ctlgrs1064797134
Max Magnitude0
ClinVar
Risk rs1064797134(A;A)
Alt rs1064797134(A;A)
Reference Rs1064797134(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216052142C>T
CLNSRC
CLNACC RCV000488256.1,