rs863225391

Orientation

plus

Stabilized

plus

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

Make rs863225391(-;-)

Make rs863225391(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47466685

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225391
dbSNP (classic)	rs863225391
ClinGen	rs863225391
ebi	rs863225391
HLI	rs863225391
Exac	rs863225391
Gnomad	rs863225391
Varsome	rs863225391
LitVar	rs863225391
Map	rs863225391
PheGenI	rs863225391
Biobank	rs863225391
1000 genomes	rs863225391
hgdp	rs863225391
ensembl	rs863225391
geneview	rs863225391
scholar	rs863225391
google	rs863225391
pharmgkb	rs863225391
gwascentral	rs863225391
openSNP	rs863225391
23andMe	rs863225391
SNPshot	rs863225391
SNPdbe	rs863225391
MSV3d	rs863225391
GWAS Ctlg	rs863225391

Max Magnitude

0

ClinVar
Risk	rs863225391(-;-)
Alt	rs863225391(-;-)
Reference	Rs863225391(TG;TG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47693824_47693825delTG
CLNSRC
CLNACC	RCV000202016.1,