rs587782265

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GCACATCGAGAGCA)	6	Lynch syndrome
(AGCAGCACATCGAG;AGCAGCACATCGAG)	0	common in clinvar

Make rs587782265(-;-)

Make rs587782265(GCACATCGAGAGCA;GCACATCGAGAGCA)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37020409

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587782265
dbSNP (classic)	rs587782265
ClinGen	rs587782265
ebi	rs587782265
HLI	rs587782265
Exac	rs587782265
Gnomad	rs587782265
Varsome	rs587782265
LitVar	rs587782265
Map	rs587782265
PheGenI	rs587782265
Biobank	rs587782265
1000 genomes	rs587782265
hgdp	rs587782265
ensembl	rs587782265
geneview	rs587782265
scholar	rs587782265
google	rs587782265
pharmgkb	rs587782265
gwascentral	rs587782265
openSNP	rs587782265
23andMe	rs587782265
SNPshot	rs587782265
SNPdbe	rs587782265
MSV3d	rs587782265
GWAS Ctlg	rs587782265

Max Magnitude

6

ClinVar
Risk	rs587782265(-;-)
Alt	rs587782265(-;-)
Reference	Rs587782265(AGCAGCACATCGAG;AGCAGCACATCGAG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37061900_37061913delGCACATCGAGAGCA
CLNSRC
CLNACC	RCV000130995.2,