rs863225392

Orientation

plus

Stabilized

plus

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

Make rs863225392(-;A)

Make rs863225392(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47478297

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225392
dbSNP (classic)	rs863225392
ClinGen	rs863225392
ebi	rs863225392
HLI	rs863225392
Exac	rs863225392
Gnomad	rs863225392
Varsome	rs863225392
LitVar	rs863225392
Map	rs863225392
PheGenI	rs863225392
Biobank	rs863225392
1000 genomes	rs863225392
hgdp	rs863225392
ensembl	rs863225392
geneview	rs863225392
scholar	rs863225392
google	rs863225392
pharmgkb	rs863225392
gwascentral	rs863225392
openSNP	rs863225392
23andMe	rs863225392
SNPshot	rs863225392
SNPdbe	rs863225392
MSV3d	rs863225392
GWAS Ctlg	rs863225392

Max Magnitude

0

ClinVar
Risk	rs863225392(A;A)
Alt	rs863225392(A;A)
Reference	Rs863225392(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47705436dupA
CLNSRC
CLNACC	RCV000202169.1,