rs587779175

Orientation

plus

Stabilized

plus

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

Make rs587779175(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47403262

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779175
dbSNP (classic)	rs587779175
ClinGen	rs587779175
ebi	rs587779175
HLI	rs587779175
Exac	rs587779175
Gnomad	rs587779175
Varsome	rs587779175
LitVar	rs587779175
Map	rs587779175
PheGenI	rs587779175
Biobank	rs587779175
1000 genomes	rs587779175
hgdp	rs587779175
ensembl	rs587779175
geneview	rs587779175
scholar	rs587779175
google	rs587779175
pharmgkb	rs587779175
gwascentral	rs587779175
openSNP	rs587779175
23andMe	rs587779175
SNPshot	rs587779175
SNPdbe	rs587779175
MSV3d	rs587779175
GWAS Ctlg	rs587779175

Max Magnitude

6

ClinVar
Risk	rs587779175(A;A)
Alt	rs587779175(A;A)
Reference	Rs587779175(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630401dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076691.2,