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rs63751431

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751431(-;-)
Make rs63751431(-;AATC)
Make rs63751431(AATC;AATC)
ReferenceGRCh38 38.1/142
Chromosome3
Position36996633
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751431
ebirs63751431
HLIrs63751431
Exacrs63751431
Varsomers63751431
Maprs63751431
PheGenIrs63751431
hapmaprs63751431
1000 genomesrs63751431
hgdprs63751431
ensemblrs63751431
gopubmedrs63751431
geneviewrs63751431
scholarrs63751431
googlers63751431
pharmgkbrs63751431
gwascentralrs63751431
openSNPrs63751431
23andMers63751431
23andMe allrs63751431
SNP Nexus

SNPshotrs63751431
SNPdbers63751431
MSV3drs63751431
GWAS Ctlgrs63751431
Max Magnitude0
ClinVar
Risk rs63751431(AATC;AATC)
Alt rs63751431(AATC;AATC)
Reference rs63751431(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038121_37038124dupAATC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075165.2,