rs63751711

Orientation

plus

Stabilized

plus

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

Make rs63751711(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37012099

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751711
dbSNP (classic)	rs63751711
ClinGen	rs63751711
ebi	rs63751711
HLI	rs63751711
Exac	rs63751711
Gnomad	rs63751711
Varsome	rs63751711
LitVar	rs63751711
Map	rs63751711
PheGenI	rs63751711
Biobank	rs63751711
1000 genomes	rs63751711
hgdp	rs63751711
ensembl	rs63751711
geneview	rs63751711
scholar	rs63751711
google	rs63751711
pharmgkb	rs63751711
gwascentral	rs63751711
openSNP	rs63751711
23andMe	rs63751711
SNPshot	rs63751711
SNPdbe	rs63751711
MSV3d	rs63751711
GWAS Ctlg	rs63751711

Max Magnitude

6

ClinVar
Risk	rs63751711(A;A) rs63751711(T;T)
Alt	rs63751711(A;A) rs63751711(T;T)
Reference	Rs63751711(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Lynch syndrome II
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Lynch syndrome II
Reversed	0
HGVS	NC_000003.11:g.37053590G>A; NC_000003.11:g.37053590G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075809.2, RCV000132197.3, RCV000202049.3, RCV000410542.1, RCV000075810.3, RCV000160555.2,