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rs1064795264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAGCGCGGCC;GAGCGCGGCC) 0 common in clinvar
Chromosome2
Position47403230
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064795264
dbSNP (old)rs1064795264
ClinGenrs1064795264
ebirs1064795264
HLIrs1064795264
Exacrs1064795264
Gnomadrs1064795264
Varsomers1064795264
Maprs1064795264
PheGenIrs1064795264
Biobankrs1064795264
1000 genomesrs1064795264
hgdprs1064795264
ensemblrs1064795264
gopubmedrs1064795264
geneviewrs1064795264
scholarrs1064795264
googlers1064795264
pharmgkbrs1064795264
gwascentralrs1064795264
openSNPrs1064795264
23andMers1064795264
23andMe allrs1064795264
SNPshotrs1064795264
SNPdbers1064795264
MSV3drs1064795264
GWAS Ctlgrs1064795264
Max Magnitude0
ClinVar
Risk rs1064795264(-;-)
Alt rs1064795264(-;-)
Reference Rs1064795264(GAGCGCGGCC;GAGCGCGGCC)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47630369_47630378delCGCGGCCGAG
CLNSRC
CLNACC RCV000486490.1,