Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608001(A;C)
Make rs267608001(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478270
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608001
ebirs267608001
HLIrs267608001
Exacrs267608001
Varsomers267608001
Maprs267608001
PheGenIrs267608001
hapmaprs267608001
1000 genomesrs267608001
hgdprs267608001
ensemblrs267608001
gopubmedrs267608001
geneviewrs267608001
scholarrs267608001
googlers267608001
pharmgkbrs267608001
gwascentralrs267608001
openSNPrs267608001
23andMers267608001
23andMe allrs267608001
SNP Nexus

SNPshotrs267608001
SNPdbers267608001
MSV3drs267608001
GWAS Ctlgrs267608001
Max Magnitude0
ClinVar
Risk rs267608001(C,G,T;C,G,T)
Alt rs267608001(C,G,T;C,G,T)
Reference rs267608001(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705409A>C; NC_000002.11:g.47705409A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076431.2, RCV000076432.2,