rs730881776

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;ATGC)	6	Lynch syndrome
(ATGC;ATGC)	0	common/normal
(GCAT;GCAT)	0	common in clinvar
(I;I)	0	common genotype

Make rs730881776(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47475181

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs730881776
dbSNP (classic)	rs730881776
ClinGen	rs730881776
ebi	rs730881776
HLI	rs730881776
Exac	rs730881776
Gnomad	rs730881776
Varsome	rs730881776
LitVar	rs730881776
Map	rs730881776
PheGenI	rs730881776
Biobank	rs730881776
1000 genomes	rs730881776
hgdp	rs730881776
ensembl	rs730881776
geneview	rs730881776
scholar	rs730881776
google	rs730881776
pharmgkb	rs730881776
gwascentral	rs730881776
openSNP	rs730881776
23andMe	rs730881776
SNPshot	rs730881776
SNPdbe	rs730881776
MSV3d	rs730881776
GWAS Ctlg	rs730881776

Max Magnitude

6

ClinVar
Risk	rs730881776(-;-)
Alt	rs730881776(-;-)
Reference	Rs730881776(GCAT;GCAT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47702320_47702323delATGC
CLNSRC
CLNACC	RCV000160631.1,