rs587779097

Orientation

plus

Stabilized

plus

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

Make rs587779097(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47466675

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779097
dbSNP (classic)	rs587779097
ClinGen	rs587779097
ebi	rs587779097
HLI	rs587779097
Exac	rs587779097
Gnomad	rs587779097
Varsome	rs587779097
LitVar	rs587779097
Map	rs587779097
PheGenI	rs587779097
Biobank	rs587779097
1000 genomes	rs587779097
hgdp	rs587779097
ensembl	rs587779097
geneview	rs587779097
scholar	rs587779097
google	rs587779097
pharmgkb	rs587779097
gwascentral	rs587779097
openSNP	rs587779097
23andMe	rs587779097
SNPshot	rs587779097
SNPdbe	rs587779097
MSV3d	rs587779097
GWAS Ctlg	rs587779097

Max Magnitude

6

ClinVar
Risk	rs587779097(T;T)
Alt	rs587779097(T;T)
Reference	Rs587779097(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47693814C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076189.2,