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rs1064797133

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome1
Position215766752
GeneUSH2A
is asnp
is mentioned by
dbSNPrs1064797133
dbSNP (old)rs1064797133
ClinGenrs1064797133
ebirs1064797133
HLIrs1064797133
Exacrs1064797133
Gnomadrs1064797133
Varsomers1064797133
Maprs1064797133
PheGenIrs1064797133
Biobankrs1064797133
1000 genomesrs1064797133
hgdprs1064797133
ensemblrs1064797133
gopubmedrs1064797133
geneviewrs1064797133
scholarrs1064797133
googlers1064797133
pharmgkbrs1064797133
gwascentralrs1064797133
openSNPrs1064797133
23andMers1064797133
23andMe allrs1064797133
SNPshotrs1064797133
SNPdbers1064797133
MSV3drs1064797133
GWAS Ctlgrs1064797133
Max Magnitude0
ClinVar
Risk rs1064797133(TA;TA)
Alt rs1064797133(TA;TA)
Reference Rs1064797133(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.215940094_215940095insTA
CLNSRC
CLNACC RCV000487538.1,