rs587778896

Orientation

plus

Stabilized

plus

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

Make rs587778896(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

36996621

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778896
dbSNP (classic)	rs587778896
ClinGen	rs587778896
ebi	rs587778896
HLI	rs587778896
Exac	rs587778896
Gnomad	rs587778896
Varsome	rs587778896
LitVar	rs587778896
Map	rs587778896
PheGenI	rs587778896
Biobank	rs587778896
1000 genomes	rs587778896
hgdp	rs587778896
ensembl	rs587778896
geneview	rs587778896
scholar	rs587778896
google	rs587778896
pharmgkb	rs587778896
gwascentral	rs587778896
openSNP	rs587778896
23andMe	rs587778896
SNPshot	rs587778896
SNPdbe	rs587778896
MSV3d	rs587778896
GWAS Ctlg	rs587778896

Max Magnitude

6

ClinVar
Risk	rs587778896(-;-)
Alt	rs587778896(-;-)
Reference	Rs587778896(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038112delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075148.2,