rs587779147

Orientation

plus

Stabilized

plus

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

Make rs587779147(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47480758

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779147
dbSNP (classic)	rs587779147
ClinGen	rs587779147
ebi	rs587779147
HLI	rs587779147
Exac	rs587779147
Gnomad	rs587779147
Varsome	rs587779147
LitVar	rs587779147
Map	rs587779147
PheGenI	rs587779147
Biobank	rs587779147
1000 genomes	rs587779147
hgdp	rs587779147
ensembl	rs587779147
geneview	rs587779147
scholar	rs587779147
google	rs587779147
pharmgkb	rs587779147
gwascentral	rs587779147
openSNP	rs587779147
23andMe	rs587779147
SNPshot	rs587779147
SNPdbe	rs587779147
MSV3d	rs587779147
GWAS Ctlg	rs587779147

Max Magnitude

6

ClinVar
Risk	rs587779147(-;-)
Alt	rs587779147(-;-)
Reference	Rs587779147(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707897delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076494.2,