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rs63750715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750715(-;-)
Make rs63750715(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025699
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750715
ebirs63750715
HLIrs63750715
Exacrs63750715
Varsomers63750715
Maprs63750715
PheGenIrs63750715
hapmaprs63750715
1000 genomesrs63750715
hgdprs63750715
ensemblrs63750715
gopubmedrs63750715
geneviewrs63750715
scholarrs63750715
googlers63750715
pharmgkbrs63750715
gwascentralrs63750715
openSNPrs63750715
23andMers63750715
23andMe allrs63750715
SNP Nexus

SNPshotrs63750715
SNPdbers63750715
MSV3drs63750715
GWAS Ctlgrs63750715
Max Magnitude0
ClinVar
Risk rs63750715(;)
Alt rs63750715(;)
Reference rs63750715(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067190delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075112.2,