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rs63751015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(D;D) 0
Make rs63751015(-;-)
Make rs63751015(-;CT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025808
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751015
ebirs63751015
HLIrs63751015
Exacrs63751015
Varsomers63751015
Maprs63751015
PheGenIrs63751015
hapmaprs63751015
1000 genomesrs63751015
hgdprs63751015
ensemblrs63751015
gopubmedrs63751015
geneviewrs63751015
scholarrs63751015
googlers63751015
pharmgkbrs63751015
gwascentralrs63751015
openSNPrs63751015
23andMers63751015
23andMe allrs63751015
SNP Nexus

SNPshotrs63751015
SNPdbers63751015
MSV3drs63751015
GWAS Ctlgrs63751015
Max Magnitude0
ClinVar
Risk rs63751015(;)
Alt rs63751015(;)
Reference rs63751015(CT;CT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067299_37067300delCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075150.2,