rs1057520735

Orientation

plus

Stabilized

plus

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

Make rs1057520735(C;G)

Make rs1057520735(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47476388

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1057520735
dbSNP (classic)	rs1057520735
ClinGen	rs1057520735
ebi	rs1057520735
HLI	rs1057520735
Exac	rs1057520735
Gnomad	rs1057520735
Varsome	rs1057520735
LitVar	rs1057520735
Map	rs1057520735
PheGenI	rs1057520735
Biobank	rs1057520735
1000 genomes	rs1057520735
hgdp	rs1057520735
ensembl	rs1057520735
geneview	rs1057520735
scholar	rs1057520735
google	rs1057520735
pharmgkb	rs1057520735
gwascentral	rs1057520735
openSNP	rs1057520735
23andMe	rs1057520735
SNPshot	rs1057520735
SNPdbe	rs1057520735
MSV3d	rs1057520735
GWAS Ctlg	rs1057520735

Max Magnitude

0

ClinVar
Risk	rs1057520735(G;G)
Alt	rs1057520735(G;G)
Reference	Rs1057520735(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47703527C>G
CLNSRC
CLNACC	RCV000438851.1,