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rs1060505035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060505035(A;A)
Make rs1060505035(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position82276183
GeneRPS23
is asnp
is mentioned by
dbSNPrs1060505035
dbSNP (old)rs1060505035
ClinGenrs1060505035
ebirs1060505035
HLIrs1060505035
Exacrs1060505035
Gnomadrs1060505035
Varsomers1060505035
Maprs1060505035
PheGenIrs1060505035
Biobankrs1060505035
1000 genomesrs1060505035
hgdprs1060505035
ensemblrs1060505035
gopubmedrs1060505035
geneviewrs1060505035
scholarrs1060505035
googlers1060505035
pharmgkbrs1060505035
gwascentralrs1060505035
openSNPrs1060505035
23andMers1060505035
23andMe allrs1060505035
SNPshotrs1060505035
SNPdbers1060505035
MSV3drs1060505035
GWAS Ctlgrs1060505035
Max Magnitude0
ClinVar
Risk rs1060505035(A;A)
Alt rs1060505035(A;A)
Reference Rs1060505035(T;T)
Significance Pathogenic
Disease MacInnes syndrome
Variation info
Gene RPS23
CLNDBN MacInnes syndrome
Reversed 1
HGVS NC_000005.9:g.81572002A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477697.1,