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rs63750447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750447(A;A)
Make rs63750447(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position37025749
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750447
ebirs63750447
HLIrs63750447
Exacrs63750447
Varsomers63750447
Maprs63750447
PheGenIrs63750447
hapmaprs63750447
1000 genomesrs63750447
hgdprs63750447
ensemblrs63750447
gopubmedrs63750447
geneviewrs63750447
scholarrs63750447
googlers63750447
pharmgkbrs63750447
gwascentralrs63750447
openSNPrs63750447
23andMers63750447
23andMe allrs63750447
SNP Nexus

SNPshotrs63750447
SNPdbers63750447
MSV3drs63750447
GWAS Ctlgrs63750447
Max Magnitude0

[PMID 25986311] Association between MutL homolog 1 polymorphisms and the risk of colorectal cancer: a meta-analysis


ClinVar
Risk rs63750447(A;A)
Alt rs63750447(A;A)
Reference rs63750447(T;T)
Significance Non-pathogenic
Disease not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Variation info
Gene MLH1
CLNDBN not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37067240T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000034537.3, RCV000075123.5, RCV000121360.1, RCV000129936.4, RCV000144609.1,