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rs1057517551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517551(-;T)
Make rs1057517551(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47798891
GeneMSH6
is asnp
is mentioned by
dbSNPrs1057517551
dbSNP (old)rs1057517551
ClinGenrs1057517551
ebirs1057517551
HLIrs1057517551
Exacrs1057517551
Gnomadrs1057517551
Varsomers1057517551
Maprs1057517551
PheGenIrs1057517551
Biobankrs1057517551
1000 genomesrs1057517551
hgdprs1057517551
ensemblrs1057517551
gopubmedrs1057517551
geneviewrs1057517551
scholarrs1057517551
googlers1057517551
pharmgkbrs1057517551
gwascentralrs1057517551
openSNPrs1057517551
23andMers1057517551
23andMe allrs1057517551
SNPshotrs1057517551
SNPdbers1057517551
MSV3drs1057517551
GWAS Ctlgrs1057517551
Max Magnitude0
ClinVar
Risk rs1057517551(T;T)
Alt rs1057517551(T;T)
Reference Rs1057517551(-;-)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026030dupT
CLNSRC
CLNACC RCV000411044.1, RCV000473148.1, RCV000482391.1, RCV000491372.1,