rs587778981

Orientation

plus

Stabilized

plus

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

Make rs587778981(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37050529

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778981
dbSNP (classic)	rs587778981
ClinGen	rs587778981
ebi	rs587778981
HLI	rs587778981
Exac	rs587778981
Gnomad	rs587778981
Varsome	rs587778981
LitVar	rs587778981
Map	rs587778981
PheGenI	rs587778981
Biobank	rs587778981
1000 genomes	rs587778981
hgdp	rs587778981
ensembl	rs587778981
geneview	rs587778981
scholar	rs587778981
google	rs587778981
pharmgkb	rs587778981
gwascentral	rs587778981
openSNP	rs587778981
23andMe	rs587778981
SNPshot	rs587778981
SNPdbe	rs587778981
MSV3d	rs587778981
GWAS Ctlg	rs587778981

Max Magnitude

6

ClinVar
Risk	rs587778981(-;-)
Alt	rs587778981(-;-)
Reference	Rs587778981(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092020_37092021delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075555.2,