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rs63751709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs63751709(-;-)
Make rs63751709(-;GT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042317
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751709
ebirs63751709
HLIrs63751709
Exacrs63751709
Varsomers63751709
Maprs63751709
PheGenIrs63751709
hapmaprs63751709
1000 genomesrs63751709
hgdprs63751709
ensemblrs63751709
gopubmedrs63751709
geneviewrs63751709
scholarrs63751709
googlers63751709
pharmgkbrs63751709
gwascentralrs63751709
openSNPrs63751709
23andMers63751709
23andMe allrs63751709
SNP Nexus

SNPshotrs63751709
SNPdbers63751709
MSV3drs63751709
GWAS Ctlgrs63751709
Max Magnitude0
ClinVar
Risk rs63751709(;)
Alt rs63751709(;)
Reference rs63751709(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083808_37083809delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075319.2,