rs587779179

Orientation

plus

Stabilized

plus

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

Make rs587779179(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412529

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779179
dbSNP (classic)	rs587779179
ClinGen	rs587779179
ebi	rs587779179
HLI	rs587779179
Exac	rs587779179
Gnomad	rs587779179
Varsome	rs587779179
LitVar	rs587779179
Map	rs587779179
PheGenI	rs587779179
Biobank	rs587779179
1000 genomes	rs587779179
hgdp	rs587779179
ensembl	rs587779179
geneview	rs587779179
scholar	rs587779179
google	rs587779179
pharmgkb	rs587779179
gwascentral	rs587779179
openSNP	rs587779179
23andMe	rs587779179
SNPshot	rs587779179
SNPdbe	rs587779179
MSV3d	rs587779179
GWAS Ctlg	rs587779179

Max Magnitude

6

ClinVar
Risk	rs587779179(-;-)
Alt	rs587779179(-;-)
Reference	Rs587779179(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639668delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076703.2,