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rs63749965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63749965(-;-)
Make rs63749965(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025748
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749965
ebirs63749965
HLIrs63749965
Exacrs63749965
Varsomers63749965
Maprs63749965
PheGenIrs63749965
hapmaprs63749965
1000 genomesrs63749965
hgdprs63749965
ensemblrs63749965
gopubmedrs63749965
geneviewrs63749965
scholarrs63749965
googlers63749965
pharmgkbrs63749965
gwascentralrs63749965
openSNPrs63749965
23andMers63749965
23andMe allrs63749965
SNP Nexus

SNPshotrs63749965
SNPdbers63749965
MSV3drs63749965
GWAS Ctlgrs63749965
Max Magnitude0
ClinVar
Risk rs63749965(;)
Alt rs63749965(;)
Reference rs63749965(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067239delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075122.2,