rs587779152

Orientation

plus

Stabilized

plus

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

Make rs587779152(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47480859

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779152
dbSNP (classic)	rs587779152
ClinGen	rs587779152
ebi	rs587779152
HLI	rs587779152
Exac	rs587779152
Gnomad	rs587779152
Varsome	rs587779152
LitVar	rs587779152
Map	rs587779152
PheGenI	rs587779152
Biobank	rs587779152
1000 genomes	rs587779152
hgdp	rs587779152
ensembl	rs587779152
geneview	rs587779152
scholar	rs587779152
google	rs587779152
pharmgkb	rs587779152
gwascentral	rs587779152
openSNP	rs587779152
23andMe	rs587779152
SNPshot	rs587779152
SNPdbe	rs587779152
MSV3d	rs587779152
GWAS Ctlg	rs587779152

Max Magnitude

6

ClinVar
Risk	rs587779152(A;A)
Alt	rs587779152(A;A)
Reference	Rs587779152(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707998T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076516.2,