rs587778943

Orientation

plus

Stabilized

plus

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

Make rs587778943(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37047535

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778943
dbSNP (classic)	rs587778943
ClinGen	rs587778943
ebi	rs587778943
HLI	rs587778943
Exac	rs587778943
Gnomad	rs587778943
Varsome	rs587778943
LitVar	rs587778943
Map	rs587778943
PheGenI	rs587778943
Biobank	rs587778943
1000 genomes	rs587778943
hgdp	rs587778943
ensembl	rs587778943
geneview	rs587778943
scholar	rs587778943
google	rs587778943
pharmgkb	rs587778943
gwascentral	rs587778943
openSNP	rs587778943
23andMe	rs587778943
SNPshot	rs587778943
SNPdbe	rs587778943
MSV3d	rs587778943
GWAS Ctlg	rs587778943

Max Magnitude

6

ClinVar
Risk	rs587778943(-;-)
Alt	rs587778943(-;-)
Reference	Rs587778943(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089026_37089027delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075349.2,