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rs1057524832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524832(C;T)
Make rs1057524832(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position148470380
GeneMBD5
is asnp
is mentioned by
dbSNPrs1057524832
dbSNP (old)rs1057524832
ClinGenrs1057524832
ebirs1057524832
HLIrs1057524832
Exacrs1057524832
Gnomadrs1057524832
Varsomers1057524832
Maprs1057524832
PheGenIrs1057524832
Biobankrs1057524832
1000 genomesrs1057524832
hgdprs1057524832
ensemblrs1057524832
gopubmedrs1057524832
geneviewrs1057524832
scholarrs1057524832
googlers1057524832
pharmgkbrs1057524832
gwascentralrs1057524832
openSNPrs1057524832
23andMers1057524832
23andMe allrs1057524832
SNPshotrs1057524832
SNPdbers1057524832
MSV3drs1057524832
GWAS Ctlgrs1057524832
Max Magnitude0
ClinVar
Risk rs1057524832(T;T)
Alt rs1057524832(T;T)
Reference Rs1057524832(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MBD5
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.149227949C>T
CLNSRC
CLNACC RCV000440721.1,