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rs267607881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATTTCTTTGGACCA;AATTTCTTTGGACCA) 0 common in clinvar
Make rs267607881(-;-)
Make rs267607881(-;AATTTCTTTGGACCA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048888
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607881
ebirs267607881
HLIrs267607881
Exacrs267607881
Varsomers267607881
Maprs267607881
PheGenIrs267607881
hapmaprs267607881
1000 genomesrs267607881
hgdprs267607881
ensemblrs267607881
gopubmedrs267607881
geneviewrs267607881
scholarrs267607881
googlers267607881
pharmgkbrs267607881
gwascentralrs267607881
openSNPrs267607881
23andMers267607881
23andMe allrs267607881
SNP Nexus

SNPshotrs267607881
SNPdbers267607881
MSV3drs267607881
GWAS Ctlgrs267607881
Max Magnitude0
ClinVar
Risk rs267607881(;)
Alt rs267607881(;)
Reference rs267607881(AATTTCTTTGGACCA;AATTTCTTTGGACCA)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090379_37090393delAATTTCTTTGGACCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075466.2,