rs587779006

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TG)	6	Lynch syndrome, pathogenic mutation
(GT;GT)	0	common in clinvar
(TG;TG)	0	common/normal

Make rs587779006(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37004466

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779006
dbSNP (classic)	rs587779006
ClinGen	rs587779006
ebi	rs587779006
HLI	rs587779006
Exac	rs587779006
Gnomad	rs587779006
Varsome	rs587779006
LitVar	rs587779006
Map	rs587779006
PheGenI	rs587779006
Biobank	rs587779006
1000 genomes	rs587779006
hgdp	rs587779006
ensembl	rs587779006
geneview	rs587779006
scholar	rs587779006
google	rs587779006
pharmgkb	rs587779006
gwascentral	rs587779006
openSNP	rs587779006
23andMe	rs587779006
SNPshot	rs587779006
SNPdbe	rs587779006
MSV3d	rs587779006
GWAS Ctlg	rs587779006

Max Magnitude

6

ClinVar
Risk	rs587779006(-;-)
Alt	rs587779006(-;-)
Reference	Rs587779006(GT;GT)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37045957_37045958delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075670.2, RCV000485841.1,