rs281864937

Orientation

plus

Stabilized

plus

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

Make rs281864937(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37028789

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs281864937
dbSNP (classic)	rs281864937
ClinGen	rs281864937
ebi	rs281864937
HLI	rs281864937
Exac	rs281864937
Gnomad	rs281864937
Varsome	rs281864937
LitVar	rs281864937
Map	rs281864937
PheGenI	rs281864937
Biobank	rs281864937
1000 genomes	rs281864937
hgdp	rs281864937
ensembl	rs281864937
geneview	rs281864937
scholar	rs281864937
google	rs281864937
pharmgkb	rs281864937
gwascentral	rs281864937
openSNP	rs281864937
23andMe	rs281864937
SNPshot	rs281864937
SNPdbe	rs281864937
MSV3d	rs281864937
GWAS Ctlg	rs281864937

Max Magnitude

6

ClinVar
Risk	rs281864937(-;-)
Alt	rs281864937(-;-)
Reference	Rs281864937(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37070280_37070281delGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075207.2,