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rs63750339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750339(-;-)
Make rs63750339(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020442
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750339
ebirs63750339
HLIrs63750339
Exacrs63750339
Varsomers63750339
Maprs63750339
PheGenIrs63750339
hapmaprs63750339
1000 genomesrs63750339
hgdprs63750339
ensemblrs63750339
gopubmedrs63750339
geneviewrs63750339
scholarrs63750339
googlers63750339
pharmgkbrs63750339
gwascentralrs63750339
openSNPrs63750339
23andMers63750339
23andMe allrs63750339
SNP Nexus

SNPshotrs63750339
SNPdbers63750339
MSV3drs63750339
GWAS Ctlgrs63750339
Max Magnitude0
ClinVar
Risk rs63750339(;)
Alt rs63750339(;)
Reference rs63750339(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061933delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075075.2,