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rs63750749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750749(-;-)
Make rs63750749(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025788
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750749
ebirs63750749
HLIrs63750749
Exacrs63750749
Varsomers63750749
Maprs63750749
PheGenIrs63750749
hapmaprs63750749
1000 genomesrs63750749
hgdprs63750749
ensemblrs63750749
gopubmedrs63750749
geneviewrs63750749
scholarrs63750749
googlers63750749
pharmgkbrs63750749
gwascentralrs63750749
openSNPrs63750749
23andMers63750749
23andMe allrs63750749
SNP Nexus

SNPshotrs63750749
SNPdbers63750749
MSV3drs63750749
GWAS Ctlgrs63750749
Max Magnitude0
ClinVar
Risk rs63750749(;)
Alt rs63750749(;)
Reference rs63750749(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067279delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075145.2, RCV000165649.1,