rs267607778

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 rs267607778(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37012100

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607778
dbSNP (classic)	rs267607778
ClinGen	rs267607778
ebi	rs267607778
HLI	rs267607778
Exac	rs267607778
Gnomad	rs267607778
Varsome	rs267607778
LitVar	rs267607778
Map	rs267607778
PheGenI	rs267607778
Biobank	rs267607778
1000 genomes	rs267607778
hgdp	rs267607778
ensembl	rs267607778
geneview	rs267607778
scholar	rs267607778
google	rs267607778
pharmgkb	rs267607778
gwascentral	rs267607778
openSNP	rs267607778
23andMe	rs267607778
SNPshot	rs267607778
SNPdbe	rs267607778
MSV3d	rs267607778
GWAS Ctlg	rs267607778

Max Magnitude

6

ClinVar
Risk	rs267607778(A;A) rs267607778(T;T)
Alt	rs267607778(A;A) rs267607778(T;T)
Reference	Rs267607778(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37053591G>A; NC_000003.11:g.37053591G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075802.2, RCV000075803.2, RCV000480845.1,