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rs267608049

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs267608049(AG;AG)
Make rs267608049(AG;TC)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799597
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608049
ebirs267608049
HLIrs267608049
Exacrs267608049
Varsomers267608049
Maprs267608049
PheGenIrs267608049
hapmaprs267608049
1000 genomesrs267608049
hgdprs267608049
ensemblrs267608049
gopubmedrs267608049
geneviewrs267608049
scholarrs267608049
googlers267608049
pharmgkbrs267608049
gwascentralrs267608049
openSNPrs267608049
23andMers267608049
23andMe allrs267608049
SNP Nexus

SNPshotrs267608049
SNPdbers267608049
MSV3drs267608049
GWAS Ctlgrs267608049
Max Magnitude0
ClinVar
Risk rs267608049(AG;AG)
Alt rs267608049(AG;AG)
Reference rs267608049(TC;TC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026736_48026737delTCinsAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074669.2,