rs267607866

Orientation

plus

Stabilized

plus

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

Make rs267607866(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

37047642

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607866
dbSNP (classic)	rs267607866
ClinGen	rs267607866
ebi	rs267607866
HLI	rs267607866
Exac	rs267607866
Gnomad	rs267607866
Varsome	rs267607866
LitVar	rs267607866
Map	rs267607866
PheGenI	rs267607866
Biobank	rs267607866
1000 genomes	rs267607866
hgdp	rs267607866
ensembl	rs267607866
geneview	rs267607866
scholar	rs267607866
google	rs267607866
pharmgkb	rs267607866
gwascentral	rs267607866
openSNP	rs267607866
23andMe	rs267607866
SNPshot	rs267607866
SNPdbe	rs267607866
MSV3d	rs267607866
GWAS Ctlg	rs267607866

Max Magnitude

6

ClinVar
Risk	rs267607866(C;C)
Alt	rs267607866(C;C)
Reference	Rs267607866(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37089133G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075387.2, RCV000165622.1,