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rs1060501151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501151(-;-)
Make rs1060501151(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position148512911
GeneMBD5
is asnp
is mentioned by
dbSNPrs1060501151
dbSNP (old)rs1060501151
ClinGenrs1060501151
ebirs1060501151
HLIrs1060501151
Exacrs1060501151
Gnomadrs1060501151
Varsomers1060501151
LitVarrs1060501151
Maprs1060501151
PheGenIrs1060501151
Biobankrs1060501151
1000 genomesrs1060501151
hgdprs1060501151
ensemblrs1060501151
gopubmedrs1060501151
geneviewrs1060501151
scholarrs1060501151
googlers1060501151
pharmgkbrs1060501151
gwascentralrs1060501151
openSNPrs1060501151
23andMers1060501151
23andMe allrs1060501151
SNPshotrs1060501151
SNPdbers1060501151
MSV3drs1060501151
GWAS Ctlgrs1060501151
Max Magnitude0
ClinVar
Risk rs1060501151(-;-)
Alt rs1060501151(-;-)
Reference Rs1060501151(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MBD5
CLNDBN Mental retardation, autosomal dominant 1
Reversed 0
HGVS NC_000002.11:g.149270480delC
CLNSRC
CLNACC RCV000470180.1,