rs267607895

Orientation

plus

Stabilized

plus

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

Make rs267607895(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050647

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607895
dbSNP (classic)	rs267607895
ClinGen	rs267607895
ebi	rs267607895
HLI	rs267607895
Exac	rs267607895
Gnomad	rs267607895
Varsome	rs267607895
LitVar	rs267607895
Map	rs267607895
PheGenI	rs267607895
Biobank	rs267607895
1000 genomes	rs267607895
hgdp	rs267607895
ensembl	rs267607895
geneview	rs267607895
scholar	rs267607895
google	rs267607895
pharmgkb	rs267607895
gwascentral	rs267607895
openSNP	rs267607895
23andMe	rs267607895
SNPshot	rs267607895
SNPdbe	rs267607895
MSV3d	rs267607895
GWAS Ctlg	rs267607895

Max Magnitude

6

ClinVar
Risk	rs267607895(C;C)
Alt	rs267607895(C;C)
Reference	Rs267607895(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092138G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075592.2,