rs587778900

Orientation

plus

Stabilized

plus

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

Make rs587778900(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025816

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778900
dbSNP (classic)	rs587778900
ClinGen	rs587778900
ebi	rs587778900
HLI	rs587778900
Exac	rs587778900
Gnomad	rs587778900
Varsome	rs587778900
LitVar	rs587778900
Map	rs587778900
PheGenI	rs587778900
Biobank	rs587778900
1000 genomes	rs587778900
hgdp	rs587778900
ensembl	rs587778900
geneview	rs587778900
scholar	rs587778900
google	rs587778900
pharmgkb	rs587778900
gwascentral	rs587778900
openSNP	rs587778900
23andMe	rs587778900
SNPshot	rs587778900
SNPdbe	rs587778900
MSV3d	rs587778900
GWAS Ctlg	rs587778900

Max Magnitude

6

ClinVar
Risk	rs587778900(-;-)
Alt	rs587778900(-;-)
Reference	Rs587778900(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067307delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075154.2,