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rs63750866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750866(C;C)
Make rs63750866(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37006992
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750866
ebirs63750866
HLIrs63750866
Exacrs63750866
Varsomers63750866
Maprs63750866
PheGenIrs63750866
hapmaprs63750866
1000 genomesrs63750866
hgdprs63750866
ensemblrs63750866
gopubmedrs63750866
geneviewrs63750866
scholarrs63750866
googlers63750866
pharmgkbrs63750866
gwascentralrs63750866
openSNPrs63750866
23andMers63750866
23andMe allrs63750866
SNP Nexus

SNPshotrs63750866
SNPdbers63750866
MSV3drs63750866
GWAS Ctlgrs63750866
Max Magnitude0
ClinVar
Risk rs63750866(C;C)
Alt rs63750866(C;C)
Reference rs63750866(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048483G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075687.2,