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rs63751704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751704(-;-)
Make rs63751704(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996707
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751704
ebirs63751704
HLIrs63751704
Exacrs63751704
Varsomers63751704
Maprs63751704
PheGenIrs63751704
hapmaprs63751704
1000 genomesrs63751704
hgdprs63751704
ensemblrs63751704
gopubmedrs63751704
geneviewrs63751704
scholarrs63751704
googlers63751704
pharmgkbrs63751704
gwascentralrs63751704
openSNPrs63751704
23andMers63751704
23andMe allrs63751704
SNP Nexus

SNPshotrs63751704
SNPdbers63751704
MSV3drs63751704
GWAS Ctlgrs63751704
Max Magnitude0
ClinVar
Risk rs63751704(;)
Alt rs63751704(;)
Reference rs63751704(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038198delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075500.2,