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rs1064797136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position216072971
GeneLOC102723833, USH2A
is asnp
is mentioned by
dbSNPrs1064797136
dbSNP (old)rs1064797136
ClinGenrs1064797136
ebirs1064797136
HLIrs1064797136
Exacrs1064797136
Gnomadrs1064797136
Varsomers1064797136
Maprs1064797136
PheGenIrs1064797136
Biobankrs1064797136
1000 genomesrs1064797136
hgdprs1064797136
ensemblrs1064797136
gopubmedrs1064797136
geneviewrs1064797136
scholarrs1064797136
googlers1064797136
pharmgkbrs1064797136
gwascentralrs1064797136
openSNPrs1064797136
23andMers1064797136
23andMe allrs1064797136
SNPshotrs1064797136
SNPdbers1064797136
MSV3drs1064797136
GWAS Ctlgrs1064797136
Max Magnitude0
ClinVar
Risk rs1064797136(C;C)
Alt rs1064797136(C;C)
Reference Rs1064797136(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102723833 USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216246313T>G
CLNSRC
CLNACC RCV000487963.1,