rs587778962

Orientation

plus

Stabilized

plus

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

Make rs587778962(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37048550

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778962
dbSNP (classic)	rs587778962
ClinGen	rs587778962
ebi	rs587778962
HLI	rs587778962
Exac	rs587778962
Gnomad	rs587778962
Varsome	rs587778962
LitVar	rs587778962
Map	rs587778962
PheGenI	rs587778962
Biobank	rs587778962
1000 genomes	rs587778962
hgdp	rs587778962
ensembl	rs587778962
geneview	rs587778962
scholar	rs587778962
google	rs587778962
pharmgkb	rs587778962
gwascentral	rs587778962
openSNP	rs587778962
23andMe	rs587778962
SNPshot	rs587778962
SNPdbe	rs587778962
MSV3d	rs587778962
GWAS Ctlg	rs587778962

Max Magnitude

6

ClinVar
Risk	rs587778962(-;-)
Alt	rs587778962(-;-)
Reference	Rs587778962(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090041delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075429.2,