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rs63750515

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750515(G;G)
Make rs63750515(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011828
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750515
ebirs63750515
HLIrs63750515
Exacrs63750515
Varsomers63750515
Maprs63750515
PheGenIrs63750515
hapmaprs63750515
1000 genomesrs63750515
hgdprs63750515
ensemblrs63750515
gopubmedrs63750515
geneviewrs63750515
scholarrs63750515
googlers63750515
pharmgkbrs63750515
gwascentralrs63750515
openSNPrs63750515
23andMers63750515
23andMe allrs63750515
SNP Nexus

SNPshotrs63750515
SNPdbers63750515
MSV3drs63750515
GWAS Ctlgrs63750515
Max Magnitude0
ClinVar
Risk rs63750515(A,G;A,G)
Alt rs63750515(A,G;A,G)
Reference rs63750515(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37053319T>A; NC_000003.11:g.37053319T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000165408.1, RCV000075761.2, RCV000218149.1,