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rs1064797138

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position216207368
GeneLOC105372918, USH2A
is asnp
is mentioned by
dbSNPrs1064797138
dbSNP (old)rs1064797138
ClinGenrs1064797138
ebirs1064797138
HLIrs1064797138
Exacrs1064797138
Gnomadrs1064797138
Varsomers1064797138
Maprs1064797138
PheGenIrs1064797138
Biobankrs1064797138
1000 genomesrs1064797138
hgdprs1064797138
ensemblrs1064797138
gopubmedrs1064797138
geneviewrs1064797138
scholarrs1064797138
googlers1064797138
pharmgkbrs1064797138
gwascentralrs1064797138
openSNPrs1064797138
23andMers1064797138
23andMe allrs1064797138
SNPshotrs1064797138
SNPdbers1064797138
MSV3drs1064797138
GWAS Ctlgrs1064797138
Max Magnitude0
ClinVar
Risk rs1064797138(A;A)
Alt rs1064797138(A;A)
Reference Rs1064797138(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216380710C>T
CLNSRC
CLNACC RCV000488319.1,