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rs63751685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751685(-;-)
Make rs63751685(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042325
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751685
ebirs63751685
HLIrs63751685
Exacrs63751685
Varsomers63751685
Maprs63751685
PheGenIrs63751685
hapmaprs63751685
1000 genomesrs63751685
hgdprs63751685
ensemblrs63751685
gopubmedrs63751685
geneviewrs63751685
scholarrs63751685
googlers63751685
pharmgkbrs63751685
gwascentralrs63751685
openSNPrs63751685
23andMers63751685
23andMe allrs63751685
SNP Nexus

SNPshotrs63751685
SNPdbers63751685
MSV3drs63751685
GWAS Ctlgrs63751685
Max Magnitude0
ClinVar
Risk rs63751685(;)
Alt rs63751685(;)
Reference rs63751685(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083816delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075321.2,