rs587778908

Orientation

plus

Stabilized

plus

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

Make rs587778908(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025975

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778908
dbSNP (classic)	rs587778908
ClinGen	rs587778908
ebi	rs587778908
HLI	rs587778908
Exac	rs587778908
Gnomad	rs587778908
Varsome	rs587778908
LitVar	rs587778908
Map	rs587778908
PheGenI	rs587778908
Biobank	rs587778908
1000 genomes	rs587778908
hgdp	rs587778908
ensembl	rs587778908
geneview	rs587778908
scholar	rs587778908
google	rs587778908
pharmgkb	rs587778908
gwascentral	rs587778908
openSNP	rs587778908
23andMe	rs587778908
SNPshot	rs587778908
SNPdbe	rs587778908
MSV3d	rs587778908
GWAS Ctlg	rs587778908

Max Magnitude

6

ClinVar
Risk	rs587778908(-;-)
Alt	rs587778908(-;-)
Reference	Rs587778908(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067466delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075182.2,