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rs63750293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750293(-;-)
Make rs63750293(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025859
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750293
ebirs63750293
HLIrs63750293
Exacrs63750293
Varsomers63750293
Maprs63750293
PheGenIrs63750293
hapmaprs63750293
1000 genomesrs63750293
hgdprs63750293
ensemblrs63750293
gopubmedrs63750293
geneviewrs63750293
scholarrs63750293
googlers63750293
pharmgkbrs63750293
gwascentralrs63750293
openSNPrs63750293
23andMers63750293
23andMe allrs63750293
SNP Nexus

SNPshotrs63750293
SNPdbers63750293
MSV3drs63750293
GWAS Ctlgrs63750293
Max Magnitude0
ClinVar
Risk rs63750293(;)
Alt rs63750293(;)
Reference rs63750293(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067350delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075162.2,