rs267607735

Orientation

plus

Stabilized

plus

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

Make rs267607735(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001058

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607735
dbSNP (classic)	rs267607735
ClinGen	rs267607735
ebi	rs267607735
HLI	rs267607735
Exac	rs267607735
Gnomad	rs267607735
Varsome	rs267607735
LitVar	rs267607735
Map	rs267607735
PheGenI	rs267607735
Biobank	rs267607735
1000 genomes	rs267607735
hgdp	rs267607735
ensembl	rs267607735
geneview	rs267607735
scholar	rs267607735
google	rs267607735
pharmgkb	rs267607735
gwascentral	rs267607735
openSNP	rs267607735
23andMe	rs267607735
SNPshot	rs267607735
SNPdbe	rs267607735
MSV3d	rs267607735
GWAS Ctlg	rs267607735

Max Magnitude

6

ClinVar
Risk	rs267607735(A;A)
Alt	rs267607735(A;A)
Reference	Rs267607735(G;G)
Significance	Pathogenic
Disease	Lynch syndrome II Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome II Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37042549G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022504.27, RCV000075634.2, RCV000202186.1,