rs587779104

Orientation

plus

Stabilized

plus

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

Make rs587779104(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47470996

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779104
dbSNP (classic)	rs587779104
ClinGen	rs587779104
ebi	rs587779104
HLI	rs587779104
Exac	rs587779104
Gnomad	rs587779104
Varsome	rs587779104
LitVar	rs587779104
Map	rs587779104
PheGenI	rs587779104
Biobank	rs587779104
1000 genomes	rs587779104
hgdp	rs587779104
ensembl	rs587779104
geneview	rs587779104
scholar	rs587779104
google	rs587779104
pharmgkb	rs587779104
gwascentral	rs587779104
openSNP	rs587779104
23andMe	rs587779104
SNPshot	rs587779104
SNPdbe	rs587779104
MSV3d	rs587779104
GWAS Ctlg	rs587779104

Max Magnitude

6

ClinVar
Risk	rs587779104(T;T)
Alt	rs587779104(T;T)
Reference	Rs587779104(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47698135A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076248.2,