rs587779032

Orientation

plus

Stabilized

plus

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

Make rs587779032(AT;AT)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37012099

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779032
dbSNP (classic)	rs587779032
ClinGen	rs587779032
ebi	rs587779032
HLI	rs587779032
Exac	rs587779032
Gnomad	rs587779032
Varsome	rs587779032
LitVar	rs587779032
Map	rs587779032
PheGenI	rs587779032
Biobank	rs587779032
1000 genomes	rs587779032
hgdp	rs587779032
ensembl	rs587779032
geneview	rs587779032
scholar	rs587779032
google	rs587779032
pharmgkb	rs587779032
gwascentral	rs587779032
openSNP	rs587779032
23andMe	rs587779032
SNPshot	rs587779032
SNPdbe	rs587779032
MSV3d	rs587779032
GWAS Ctlg	rs587779032

Max Magnitude

6

ClinVar
Risk	rs587779032(AT;AT)
Alt	rs587779032(AT;AT)
Reference	Rs587779032(GG;GG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37053590_37053591delGGinsAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075811.2,