rs267607720

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6	Likely miscall in v5 23andMe data or v2 Ancestry data; otherwise, Lynch syndrome, pathogenic mutation
(C;T)	6	Lynch syndrome

Make rs267607720(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37000952

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607720
dbSNP (classic)	rs267607720
ClinGen	rs267607720
ebi	rs267607720
HLI	rs267607720
Exac	rs267607720
Gnomad	rs267607720
Varsome	rs267607720
LitVar	rs267607720
Map	rs267607720
PheGenI	rs267607720
Biobank	rs267607720
1000 genomes	rs267607720
hgdp	rs267607720
ensembl	rs267607720
geneview	rs267607720
scholar	rs267607720
google	rs267607720
pharmgkb	rs267607720
gwascentral	rs267607720
openSNP	rs267607720
23andMe	rs267607720
SNPshot	rs267607720
SNPdbe	rs267607720
MSV3d	rs267607720
GWAS Ctlg	rs267607720

Max Magnitude

6

aka c.208-3C>G

ClinVar
Risk	rs267607720(G;G)
Alt	rs267607720(G;G)
Reference	Rs267607720(C;C)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37042443C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075517.2, RCV000160554.2,