rs587779042

Orientation

plus

Stabilized

plus

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

Make rs587779042(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37017499

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779042
dbSNP (classic)	rs587779042
ClinGen	rs587779042
ebi	rs587779042
HLI	rs587779042
Exac	rs587779042
Gnomad	rs587779042
Varsome	rs587779042
LitVar	rs587779042
Map	rs587779042
PheGenI	rs587779042
Biobank	rs587779042
1000 genomes	rs587779042
hgdp	rs587779042
ensembl	rs587779042
geneview	rs587779042
scholar	rs587779042
google	rs587779042
pharmgkb	rs587779042
gwascentral	rs587779042
openSNP	rs587779042
23andMe	rs587779042
SNPshot	rs587779042
SNPdbe	rs587779042
MSV3d	rs587779042
GWAS Ctlg	rs587779042

Max Magnitude

6

ClinVar
Risk	rs587779042(A;A)
Alt	rs587779042(A;A)
Reference	Rs587779042(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37058990T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075866.2,