rs587779022

Orientation

plus

Stabilized

plus

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

Make rs587779022(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37011819

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779022
dbSNP (classic)	rs587779022
ClinGen	rs587779022
ebi	rs587779022
HLI	rs587779022
Exac	rs587779022
Gnomad	rs587779022
Varsome	rs587779022
LitVar	rs587779022
Map	rs587779022
PheGenI	rs587779022
Biobank	rs587779022
1000 genomes	rs587779022
hgdp	rs587779022
ensembl	rs587779022
geneview	rs587779022
scholar	rs587779022
google	rs587779022
pharmgkb	rs587779022
gwascentral	rs587779022
openSNP	rs587779022
23andMe	rs587779022
SNPshot	rs587779022
SNPdbe	rs587779022
MSV3d	rs587779022
GWAS Ctlg	rs587779022

Max Magnitude

6

ClinVar
Risk	rs587779022(A;A) rs587779022(C;C)
Alt	rs587779022(A;A) rs587779022(C;C)
Reference	Rs587779022(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37053310G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075754.2, RCV000482173.1,