rs267607996

Orientation

plus

Stabilized

plus

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

Make rs267607996(C;C)

Make rs267607996(C;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

47476382

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607996
dbSNP (classic)	rs267607996
ClinGen	rs267607996
ebi	rs267607996
HLI	rs267607996
Exac	rs267607996
Gnomad	rs267607996
Varsome	rs267607996
LitVar	rs267607996
Map	rs267607996
PheGenI	rs267607996
Biobank	rs267607996
1000 genomes	rs267607996
hgdp	rs267607996
ensembl	rs267607996
geneview	rs267607996
scholar	rs267607996
google	rs267607996
pharmgkb	rs267607996
gwascentral	rs267607996
openSNP	rs267607996
23andMe	rs267607996
SNPshot	rs267607996
SNPdbe	rs267607996
MSV3d	rs267607996
GWAS Ctlg	rs267607996

Max Magnitude

6

ClinVar
Risk	rs267607996(A;A) rs267607996(C;C)
Alt	rs267607996(A;A) rs267607996(C;C)
Reference	Rs267607996(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47703521G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076363.2, RCV000254985.1,