rs11541859

Orientation

plus

Stabilized

plus

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

Make rs11541859(C;C)

Make rs11541859(C;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001012

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs11541859
dbSNP (classic)	rs11541859
ClinGen	rs11541859
ebi	rs11541859
HLI	rs11541859
Exac	rs11541859
Gnomad	rs11541859
Varsome	rs11541859
LitVar	rs11541859
Map	rs11541859
PheGenI	rs11541859
Biobank	rs11541859
1000 genomes	rs11541859
hgdp	rs11541859
ensembl	rs11541859
geneview	rs11541859
scholar	rs11541859
google	rs11541859
pharmgkb	rs11541859
gwascentral	rs11541859
openSNP	rs11541859
23andMe	rs11541859
SNPshot	rs11541859
SNPdbe	rs11541859
MSV3d	rs11541859
GWAS Ctlg	rs11541859

Max Magnitude

6

?	(C;C) (C;G) (G;G)	28

ClinVar
Risk	rs11541859(C;C) rs11541859(T;T)
Alt	rs11541859(C;C) rs11541859(T;T)
Reference	Rs11541859(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37042503G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075610.2,