rs587779119

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TA)	6	Lynch syndrome, pathogenic mutation
(AT;AT)	0	common in clinvar
(TA;TA)	0	common/normal

Make rs587779119(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47475245

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779119
dbSNP (classic)	rs587779119
ClinGen	rs587779119
ebi	rs587779119
HLI	rs587779119
Exac	rs587779119
Gnomad	rs587779119
Varsome	rs587779119
LitVar	rs587779119
Map	rs587779119
PheGenI	rs587779119
Biobank	rs587779119
1000 genomes	rs587779119
hgdp	rs587779119
ensembl	rs587779119
geneview	rs587779119
scholar	rs587779119
google	rs587779119
pharmgkb	rs587779119
gwascentral	rs587779119
openSNP	rs587779119
23andMe	rs587779119
SNPshot	rs587779119
SNPdbe	rs587779119
MSV3d	rs587779119
GWAS Ctlg	rs587779119

Max Magnitude

6

ClinVar
Risk	rs587779119(-;-) Rs587779119(TA;TA)
Alt	rs587779119(-;-) Rs587779119(TA;TA)
Reference	Rs587779119(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702384_47702385delTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076328.2,