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

rs267607756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs267607756(-;-)
Make rs267607756(-;AA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008862
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607756
ebirs267607756
HLIrs267607756
Exacrs267607756
Varsomers267607756
Maprs267607756
PheGenIrs267607756
hapmaprs267607756
1000 genomesrs267607756
hgdprs267607756
ensemblrs267607756
gopubmedrs267607756
geneviewrs267607756
scholarrs267607756
googlers267607756
pharmgkbrs267607756
gwascentralrs267607756
openSNPrs267607756
23andMers267607756
23andMe allrs267607756
SNP Nexus

SNPshotrs267607756
SNPdbers267607756
MSV3drs267607756
GWAS Ctlgrs267607756
Max Magnitude0
ClinVar
Risk rs267607756(;)
Alt rs267607756(;)
Reference rs267607756(AA;AA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050353_37050354delAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075738.2,