rs63751665

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;G)	6	Lynch syndrome, pathogenic mutation
(G;G)	0	common in clinvar
(G;T)	6	Lynch syndrome, pathogenic mutation

Make rs63751665(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001053

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751665
dbSNP (classic)	rs63751665
ClinGen	rs63751665
ebi	rs63751665
HLI	rs63751665
Exac	rs63751665
Gnomad	rs63751665
Varsome	rs63751665
LitVar	rs63751665
Map	rs63751665
PheGenI	rs63751665
Biobank	rs63751665
1000 genomes	rs63751665
hgdp	rs63751665
ensembl	rs63751665
geneview	rs63751665
scholar	rs63751665
google	rs63751665
pharmgkb	rs63751665
gwascentral	rs63751665
openSNP	rs63751665
23andMe	rs63751665
SNPshot	rs63751665
SNPdbe	rs63751665
MSV3d	rs63751665
GWAS Ctlg	rs63751665

Max Magnitude

6

ClinVar
Risk	rs63751665(A;A) rs63751665(C;C) rs63751665(T;T)
Alt	rs63751665(A;A) rs63751665(C;C) rs63751665(T;T)
Reference	Rs63751665(G;G)
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.37042544G>A; NC_000003.11:g.37042544G>C; NC_000003.11:g.37042544G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000215920.1, RCV000075636.2, RCV000075637.2, RCV000115480.3, RCV000216647.1,