Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057524910

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs1057524910(-;-)
Make rs1057524910(-;GAAA)
Make rs1057524910(GAAA;GAAA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47471041
GeneMSH2
is asnp
is mentioned by
dbSNPrs1057524910
dbSNP (old)rs1057524910
ClinGenrs1057524910
ebirs1057524910
HLIrs1057524910
Exacrs1057524910
Gnomadrs1057524910
Varsomers1057524910
Maprs1057524910
PheGenIrs1057524910
Biobankrs1057524910
1000 genomesrs1057524910
hgdprs1057524910
ensemblrs1057524910
gopubmedrs1057524910
geneviewrs1057524910
scholarrs1057524910
googlers1057524910
pharmgkbrs1057524910
gwascentralrs1057524910
openSNPrs1057524910
23andMers1057524910
23andMe allrs1057524910
SNPshotrs1057524910
SNPdbers1057524910
MSV3drs1057524910
GWAS Ctlgrs1057524910
Max Magnitude0
ClinVar
Risk rs1057524910(-;-)
Alt rs1057524910(-;-)
Reference Rs1057524910(AAAG;AAAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47698180_47698183delGAAA
CLNSRC
CLNACC RCV000445447.1,