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rs63750317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750317(-;-)
Make rs63750317(-;T)
Make rs63750317(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028916
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750317
ebirs63750317
HLIrs63750317
Exacrs63750317
Varsomers63750317
Maprs63750317
PheGenIrs63750317
hapmaprs63750317
1000 genomesrs63750317
hgdprs63750317
ensemblrs63750317
gopubmedrs63750317
geneviewrs63750317
scholarrs63750317
googlers63750317
pharmgkbrs63750317
gwascentralrs63750317
openSNPrs63750317
23andMers63750317
23andMe allrs63750317
SNP Nexus

SNPshotrs63750317
SNPdbers63750317
MSV3drs63750317
GWAS Ctlgrs63750317
Max Magnitude0
ClinVar
Risk rs63750317(T;T)
Alt rs63750317(T;T)
Reference rs63750317(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070407dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075238.2,