rs267607903

Orientation

plus

Stabilized

plus

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

Make rs267607903(AACA;AACA)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050580

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607903
dbSNP (classic)	rs267607903
ClinGen	rs267607903
ebi	rs267607903
HLI	rs267607903
Exac	rs267607903
Gnomad	rs267607903
Varsome	rs267607903
LitVar	rs267607903
Map	rs267607903
PheGenI	rs267607903
Biobank	rs267607903
1000 genomes	rs267607903
hgdp	rs267607903
ensembl	rs267607903
geneview	rs267607903
scholar	rs267607903
google	rs267607903
pharmgkb	rs267607903
gwascentral	rs267607903
openSNP	rs267607903
23andMe	rs267607903
SNPshot	rs267607903
SNPdbe	rs267607903
MSV3d	rs267607903
GWAS Ctlg	rs267607903

Max Magnitude

6

ClinVar
Risk	rs267607903(AAAC;AAAC) rs267607903(AACA;AACA)
Alt	rs267607903(AAAC;AAAC) rs267607903(AACA;AACA)
Reference	Rs267607903(-;-)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37092068_37092071dupAACA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075574.2, RCV000202055.1,