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rs1064797153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGCCGCAG;AGCCGCAG) 0 common in clinvar
Chromosome11
Position17523239
GeneUSH1C
is asnp
is mentioned by
dbSNPrs1064797153
dbSNP (old)rs1064797153
ClinGenrs1064797153
ebirs1064797153
HLIrs1064797153
Exacrs1064797153
Gnomadrs1064797153
Varsomers1064797153
LitVarrs1064797153
Maprs1064797153
PheGenIrs1064797153
Biobankrs1064797153
1000 genomesrs1064797153
hgdprs1064797153
ensemblrs1064797153
gopubmedrs1064797153
geneviewrs1064797153
scholarrs1064797153
googlers1064797153
pharmgkbrs1064797153
gwascentralrs1064797153
openSNPrs1064797153
23andMers1064797153
23andMe allrs1064797153
SNPshotrs1064797153
SNPdbers1064797153
MSV3drs1064797153
GWAS Ctlgrs1064797153
Max Magnitude0
ClinVar
Risk rs1064797153(-;-)
Alt rs1064797153(-;-)
Reference Rs1064797153(AGCCGCAG;AGCCGCAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH1C
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.17544786_17544793delCTGCGGCT
CLNSRC
CLNACC RCV000487515.1,