rs786204320

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GGTTG;GGTTG)	0	common in clinvar

Make rs786204320(AAATTAAGA;AAATTAAGA)

Make rs786204320(AAATTAAGA;GGTTG)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47414268

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786204320
dbSNP (classic)	rs786204320
ClinGen	rs786204320
ebi	rs786204320
HLI	rs786204320
Exac	rs786204320
Gnomad	rs786204320
Varsome	rs786204320
LitVar	rs786204320
Map	rs786204320
PheGenI	rs786204320
Biobank	rs786204320
1000 genomes	rs786204320
hgdp	rs786204320
ensembl	rs786204320
geneview	rs786204320
scholar	rs786204320
google	rs786204320
pharmgkb	rs786204320
gwascentral	rs786204320
openSNP	rs786204320
23andMe	rs786204320
SNPshot	rs786204320
SNPdbe	rs786204320
MSV3d	rs786204320
GWAS Ctlg	rs786204320

Max Magnitude

0

ClinVar
Risk	rs786204320(AAATTAAGA;AAATTAAGA)
Alt	rs786204320(AAATTAAGA;AAATTAAGA)
Reference	Rs786204320(GGTTG;GGTTG)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641407_47641411delinsAAATTAAGA
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000168726.2,