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rs63750152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750152(-;-)
Make rs63750152(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047664
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750152
ebirs63750152
HLIrs63750152
Exacrs63750152
Varsomers63750152
Maprs63750152
PheGenIrs63750152
hapmaprs63750152
1000 genomesrs63750152
hgdprs63750152
ensemblrs63750152
gopubmedrs63750152
geneviewrs63750152
scholarrs63750152
googlers63750152
pharmgkbrs63750152
gwascentralrs63750152
openSNPrs63750152
23andMers63750152
23andMe allrs63750152
SNP Nexus

SNPshotrs63750152
SNPdbers63750152
MSV3drs63750152
GWAS Ctlgrs63750152
Max Magnitude0
ClinVar
Risk rs63750152(;)
Alt rs63750152(;)
Reference rs63750152(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089155delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075396.2,