Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518567

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518567(-;-)
Make rs1057518567(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position148469754
GeneMBD5
is asnp
is mentioned by
dbSNPrs1057518567
dbSNP (old)rs1057518567
ClinGenrs1057518567
ebirs1057518567
HLIrs1057518567
Exacrs1057518567
Gnomadrs1057518567
Varsomers1057518567
Maprs1057518567
PheGenIrs1057518567
Biobankrs1057518567
1000 genomesrs1057518567
hgdprs1057518567
ensemblrs1057518567
gopubmedrs1057518567
geneviewrs1057518567
scholarrs1057518567
googlers1057518567
pharmgkbrs1057518567
gwascentralrs1057518567
openSNPrs1057518567
23andMers1057518567
23andMe allrs1057518567
SNPshotrs1057518567
SNPdbers1057518567
MSV3drs1057518567
GWAS Ctlgrs1057518567
Max Magnitude0
ClinVar
Risk rs1057518567(-;-)
Alt rs1057518567(-;-)
Reference Rs1057518567(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MBD5
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.149227323delA
CLNSRC
CLNACC RCV000413134.1,