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rs63750658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750658(-;-)
Make rs63750658(-;AA)
Make rs63750658(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004449
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750658
ebirs63750658
HLIrs63750658
Exacrs63750658
Varsomers63750658
Maprs63750658
PheGenIrs63750658
hapmaprs63750658
1000 genomesrs63750658
hgdprs63750658
ensemblrs63750658
gopubmedrs63750658
geneviewrs63750658
scholarrs63750658
googlers63750658
pharmgkbrs63750658
gwascentralrs63750658
openSNPrs63750658
23andMers63750658
23andMe allrs63750658
SNP Nexus

SNPshotrs63750658
SNPdbers63750658
MSV3drs63750658
GWAS Ctlgrs63750658
Max Magnitude0
ClinVar
Risk rs63750658(AA;AA)
Alt rs63750658(AA;AA)
Reference rs63750658(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045939_37045940dupAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075667.2,