rs587779079

Orientation

plus

Stabilized

plus

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

Make rs587779079(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47429914

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779079
dbSNP (classic)	rs587779079
ClinGen	rs587779079
ebi	rs587779079
HLI	rs587779079
Exac	rs587779079
Gnomad	rs587779079
Varsome	rs587779079
LitVar	rs587779079
Map	rs587779079
PheGenI	rs587779079
Biobank	rs587779079
1000 genomes	rs587779079
hgdp	rs587779079
ensembl	rs587779079
geneview	rs587779079
scholar	rs587779079
google	rs587779079
pharmgkb	rs587779079
gwascentral	rs587779079
openSNP	rs587779079
23andMe	rs587779079
SNPshot	rs587779079
SNPdbe	rs587779079
MSV3d	rs587779079
GWAS Ctlg	rs587779079

Max Magnitude

6

ClinVar
Risk	rs587779079(-;-)
Alt	rs587779079(-;-)
Reference	Rs587779079(ATGTT;ATGTT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47657053_47657057delGTTAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076077.2,