rs730881775

Orientation

plus

Stabilized

plus

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

Make rs730881775(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47403202

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs730881775
dbSNP (classic)	rs730881775
ClinGen	rs730881775
ebi	rs730881775
HLI	rs730881775
Exac	rs730881775
Gnomad	rs730881775
Varsome	rs730881775
LitVar	rs730881775
Map	rs730881775
PheGenI	rs730881775
Biobank	rs730881775
1000 genomes	rs730881775
hgdp	rs730881775
ensembl	rs730881775
geneview	rs730881775
scholar	rs730881775
google	rs730881775
pharmgkb	rs730881775
gwascentral	rs730881775
openSNP	rs730881775
23andMe	rs730881775
SNPshot	rs730881775
SNPdbe	rs730881775
MSV3d	rs730881775
GWAS Ctlg	rs730881775

Max Magnitude

6

ClinVar
Risk	rs730881775(A;A)
Alt	rs730881775(A;A)
Reference	Rs730881775(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47630341dup; NC_000002.11:g.47630341dupA
CLNSRC
CLNACC	RCV000491987.1, RCV000160630.2,