rs267607864

Orientation

plus

Stabilized

plus

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

Make rs267607864(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047610

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607864
dbSNP (classic)	rs267607864
ClinGen	rs267607864
ebi	rs267607864
HLI	rs267607864
Exac	rs267607864
Gnomad	rs267607864
Varsome	rs267607864
LitVar	rs267607864
Map	rs267607864
PheGenI	rs267607864
Biobank	rs267607864
1000 genomes	rs267607864
hgdp	rs267607864
ensembl	rs267607864
geneview	rs267607864
scholar	rs267607864
google	rs267607864
pharmgkb	rs267607864
gwascentral	rs267607864
openSNP	rs267607864
23andMe	rs267607864
SNPshot	rs267607864
SNPdbe	rs267607864
MSV3d	rs267607864
GWAS Ctlg	rs267607864

Max Magnitude

6

ClinVar
Risk	rs267607864(A;A) rs267607864(T;T)
Alt	rs267607864(A;A) rs267607864(T;T)
Reference	Rs267607864(C;C)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.37089101C>A; NC_000003.11:g.37089101C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075374.2, RCV000221100.1, RCV000474071.1, RCV000484604.1,