rs876658996

Orientation

plus

Stabilized

plus

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

Make rs876658996(G;G)

Make rs876658996(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47410374

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs876658996
dbSNP (classic)	rs876658996
ClinGen	rs876658996
ebi	rs876658996
HLI	rs876658996
Exac	rs876658996
Gnomad	rs876658996
Varsome	rs876658996
LitVar	rs876658996
Map	rs876658996
PheGenI	rs876658996
Biobank	rs876658996
1000 genomes	rs876658996
hgdp	rs876658996
ensembl	rs876658996
geneview	rs876658996
scholar	rs876658996
google	rs876658996
pharmgkb	rs876658996
gwascentral	rs876658996
openSNP	rs876658996
23andMe	rs876658996
SNPshot	rs876658996
SNPdbe	rs876658996
MSV3d	rs876658996
GWAS Ctlg	rs876658996

Max Magnitude

0

ClinVar
Risk	rs876658996(G;G)
Alt	rs876658996(G;G)
Reference	Rs876658996(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47637513T>G
CLNSRC
CLNACC	RCV000218166.2,