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rs63751465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751465(A;A)
Make rs63751465(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996696
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751465
ebirs63751465
HLIrs63751465
Exacrs63751465
Varsomers63751465
Maprs63751465
PheGenIrs63751465
hapmaprs63751465
1000 genomesrs63751465
hgdprs63751465
ensemblrs63751465
gopubmedrs63751465
geneviewrs63751465
scholarrs63751465
googlers63751465
pharmgkbrs63751465
gwascentralrs63751465
openSNPrs63751465
23andMers63751465
23andMe allrs63751465
SNP Nexus

SNPshotrs63751465
SNPdbers63751465
MSV3drs63751465
GWAS Ctlgrs63751465
Max Magnitude0
ClinVar
Risk rs63751465(A,T;A,T)
Alt rs63751465(A,T;A,T)
Reference rs63751465(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37038187G>A; NC_000003.11:g.37038187G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075435.2, RCV000202218.1,