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rs63751682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751682(A;G)
Make rs63751682(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048608
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751682
ebirs63751682
HLIrs63751682
Exacrs63751682
Varsomers63751682
Maprs63751682
PheGenIrs63751682
hapmaprs63751682
1000 genomesrs63751682
hgdprs63751682
ensemblrs63751682
gopubmedrs63751682
geneviewrs63751682
scholarrs63751682
googlers63751682
pharmgkbrs63751682
gwascentralrs63751682
openSNPrs63751682
23andMers63751682
23andMe allrs63751682
SNP Nexus

SNPshotrs63751682
SNPdbers63751682
MSV3drs63751682
GWAS Ctlgrs63751682
Max Magnitude0
ClinVar
Risk rs63751682(C,G;C,G)
Alt rs63751682(C,G;C,G)
Reference rs63751682(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37090099A>C; NC_000003.11:g.37090099A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075452.2, RCV000075453.2, RCV000218482.1,