rs587782537

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GAAA)	6	Lynch syndrome
(AGAA;AGAA)	0	common in clinvar
(GAAA;GAAA)	0	common/normal

Make rs587782537(-;-)

Make rs587782537(-;AGAA)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412443

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587782537
dbSNP (classic)	rs587782537
ClinGen	rs587782537
ebi	rs587782537
HLI	rs587782537
Exac	rs587782537
Gnomad	rs587782537
Varsome	rs587782537
LitVar	rs587782537
Map	rs587782537
PheGenI	rs587782537
Biobank	rs587782537
1000 genomes	rs587782537
hgdp	rs587782537
ensembl	rs587782537
geneview	rs587782537
scholar	rs587782537
google	rs587782537
pharmgkb	rs587782537
gwascentral	rs587782537
openSNP	rs587782537
23andMe	rs587782537
SNPshot	rs587782537
SNPdbe	rs587782537
MSV3d	rs587782537
GWAS Ctlg	rs587782537

Max Magnitude

6

ClinVar
Risk	rs587782537(-;-)
Alt	rs587782537(-;-)
Reference	Rs587782537(AGAA;AGAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47639582_47639585delAGAA
CLNSRC
CLNACC	RCV000131741.2,