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rs1064795629

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47806204
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064795629
dbSNP (old)rs1064795629
ClinGenrs1064795629
ebirs1064795629
HLIrs1064795629
Exacrs1064795629
Gnomadrs1064795629
Varsomers1064795629
Maprs1064795629
PheGenIrs1064795629
Biobankrs1064795629
1000 genomesrs1064795629
hgdprs1064795629
ensemblrs1064795629
gopubmedrs1064795629
geneviewrs1064795629
scholarrs1064795629
googlers1064795629
pharmgkbrs1064795629
gwascentralrs1064795629
openSNPrs1064795629
23andMers1064795629
23andMe allrs1064795629
SNPshotrs1064795629
SNPdbers1064795629
MSV3drs1064795629
GWAS Ctlgrs1064795629
Max Magnitude0
ClinVar
Risk rs1064795629(-;-)
Alt rs1064795629(-;-)
Reference Rs1064795629(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033343delG
CLNSRC
CLNACC RCV000481123.1, RCV000491618.1,