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rs63750865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750865(-;-)
Make rs63750865(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37006992
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750865
ebirs63750865
HLIrs63750865
Exacrs63750865
Varsomers63750865
Maprs63750865
PheGenIrs63750865
hapmaprs63750865
1000 genomesrs63750865
hgdprs63750865
ensemblrs63750865
gopubmedrs63750865
geneviewrs63750865
scholarrs63750865
googlers63750865
pharmgkbrs63750865
gwascentralrs63750865
openSNPrs63750865
23andMers63750865
23andMe allrs63750865
SNP Nexus

SNPshotrs63750865
SNPdbers63750865
MSV3drs63750865
GWAS Ctlgrs63750865
Max Magnitude0
ClinVar
Risk rs63750865(;)
Alt rs63750865(;)
Reference rs63750865(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048483delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075689.2,