rs587781531

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs587781531(-;-)

Make rs587781531(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47471000

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587781531
dbSNP (classic)	rs587781531
ClinGen	rs587781531
ebi	rs587781531
HLI	rs587781531
Exac	rs587781531
Gnomad	rs587781531
Varsome	rs587781531
LitVar	rs587781531
Map	rs587781531
PheGenI	rs587781531
Biobank	rs587781531
1000 genomes	rs587781531
hgdp	rs587781531
ensembl	rs587781531
geneview	rs587781531
scholar	rs587781531
google	rs587781531
pharmgkb	rs587781531
gwascentral	rs587781531
openSNP	rs587781531
23andMe	rs587781531
SNPshot	rs587781531
SNPdbe	rs587781531
MSV3d	rs587781531
GWAS Ctlg	rs587781531

Max Magnitude

0

ClinVar
Risk	rs587781531(-;-)
Alt	rs587781531(-;-)
Reference	Rs587781531(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47698139delA
CLNSRC
CLNACC	RCV000129525.3,