rs267607750

Orientation

plus

Stabilized

plus

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

Make rs267607750(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37007064

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607750
dbSNP (classic)	rs267607750
ClinGen	rs267607750
ebi	rs267607750
HLI	rs267607750
Exac	rs267607750
Gnomad	rs267607750
Varsome	rs267607750
LitVar	rs267607750
Map	rs267607750
PheGenI	rs267607750
Biobank	rs267607750
1000 genomes	rs267607750
hgdp	rs267607750
ensembl	rs267607750
geneview	rs267607750
scholar	rs267607750
google	rs267607750
pharmgkb	rs267607750
gwascentral	rs267607750
openSNP	rs267607750
23andMe	rs267607750
SNPshot	rs267607750
SNPdbe	rs267607750
MSV3d	rs267607750
GWAS Ctlg	rs267607750

Max Magnitude

6

ClinVar
Risk	rs267607750(T;T)
Alt	rs267607750(T;T)
Reference	Rs267607750(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37048555G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075712.2, RCV000160522.3,