rs587779103

Orientation

plus

Stabilized

plus

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

Make rs587779103(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47470990

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779103
dbSNP (classic)	rs587779103
ClinGen	rs587779103
ebi	rs587779103
HLI	rs587779103
Exac	rs587779103
Gnomad	rs587779103
Varsome	rs587779103
LitVar	rs587779103
Map	rs587779103
PheGenI	rs587779103
Biobank	rs587779103
1000 genomes	rs587779103
hgdp	rs587779103
ensembl	rs587779103
geneview	rs587779103
scholar	rs587779103
google	rs587779103
pharmgkb	rs587779103
gwascentral	rs587779103
openSNP	rs587779103
23andMe	rs587779103
SNPshot	rs587779103
SNPdbe	rs587779103
MSV3d	rs587779103
GWAS Ctlg	rs587779103

Max Magnitude

6

ClinVar
Risk	rs587779103(T;T)
Alt	rs587779103(T;T)
Reference	Rs587779103(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47698129dup; NC_000002.11:g.47698129dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000490897.1, RCV000076245.2,