rs587779058

Orientation

plus

Stabilized

plus

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

Make rs587779058(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37020407

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779058
dbSNP (classic)	rs587779058
ClinGen	rs587779058
ebi	rs587779058
HLI	rs587779058
Exac	rs587779058
Gnomad	rs587779058
Varsome	rs587779058
LitVar	rs587779058
Map	rs587779058
PheGenI	rs587779058
Biobank	rs587779058
1000 genomes	rs587779058
hgdp	rs587779058
ensembl	rs587779058
geneview	rs587779058
scholar	rs587779058
google	rs587779058
pharmgkb	rs587779058
gwascentral	rs587779058
openSNP	rs587779058
23andMe	rs587779058
SNPshot	rs587779058
SNPdbe	rs587779058
MSV3d	rs587779058
GWAS Ctlg	rs587779058

Max Magnitude

6

ClinVar
Risk	rs587779058(T;T)
Alt	rs587779058(T;T)
Reference	Rs587779058(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37061898C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075952.2, RCV000166394.1,