rs63750447

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs63750447(A;A)

Make rs63750447(A;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

37025749

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750447
dbSNP (classic)	rs63750447
ClinGen	rs63750447
ebi	rs63750447
HLI	rs63750447
Exac	rs63750447
Gnomad	rs63750447
Varsome	rs63750447
LitVar	rs63750447
Map	rs63750447
PheGenI	rs63750447
Biobank	rs63750447
1000 genomes	rs63750447
hgdp	rs63750447
ensembl	rs63750447
geneview	rs63750447
scholar	rs63750447
google	rs63750447
pharmgkb	rs63750447
gwascentral	rs63750447
openSNP	rs63750447
23andMe	rs63750447
SNPshot	rs63750447
SNPdbe	rs63750447
MSV3d	rs63750447
GWAS Ctlg	rs63750447

Max Magnitude

0

[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	Probable-Pathogenic
Disease	not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I Adenocarcinoma of stomach Adenocarcinoma of lung
Variation	info
Gene	MLH1
CLNDBN	not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I Adenocarcinoma of stomach Adenocarcinoma of lung
Reversed	0
HGVS	NC_000003.11:g.37067240T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000034537.3, RCV000075123.6, RCV000121360.2, RCV000129936.4, RCV000144609.1, RCV000420168.1, RCV000437810.1,