rs587779979

Orientation

plus

Stabilized

plus

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

Make rs587779979(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47414408

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779979
dbSNP (classic)	rs587779979
ClinGen	rs587779979
ebi	rs587779979
HLI	rs587779979
Exac	rs587779979
Gnomad	rs587779979
Varsome	rs587779979
LitVar	rs587779979
Map	rs587779979
PheGenI	rs587779979
Biobank	rs587779979
1000 genomes	rs587779979
hgdp	rs587779979
ensembl	rs587779979
geneview	rs587779979
scholar	rs587779979
google	rs587779979
pharmgkb	rs587779979
gwascentral	rs587779979
openSNP	rs587779979
23andMe	rs587779979
SNPshot	rs587779979
SNPdbe	rs587779979
MSV3d	rs587779979
GWAS Ctlg	rs587779979

Max Magnitude

6

ClinVar
Risk	rs587779979(-;-)
Alt	rs587779979(-;-)
Reference	Rs587779979(A;A)
Significance	Pathogenic
Disease	not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47641547delA
CLNSRC
CLNACC	RCV000115548.3, RCV000232943.1, RCV000491121.1,