rs587778987

Orientation

plus

Stabilized

plus

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

Make rs587778987(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37050563

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778987
dbSNP (classic)	rs587778987
ClinGen	rs587778987
ebi	rs587778987
HLI	rs587778987
Exac	rs587778987
Gnomad	rs587778987
Varsome	rs587778987
LitVar	rs587778987
Map	rs587778987
PheGenI	rs587778987
Biobank	rs587778987
1000 genomes	rs587778987
hgdp	rs587778987
ensembl	rs587778987
geneview	rs587778987
scholar	rs587778987
google	rs587778987
pharmgkb	rs587778987
gwascentral	rs587778987
openSNP	rs587778987
23andMe	rs587778987
SNPshot	rs587778987
SNPdbe	rs587778987
MSV3d	rs587778987
GWAS Ctlg	rs587778987

Max Magnitude

6

ClinVar
Risk	rs587778987(-;-)
Alt	rs587778987(-;-)
Reference	Rs587778987(CA;CA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092054_37092055delCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075570.2,