rs587779975

Orientation

plus

Stabilized

plus

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

Make rs587779975(-;-)

Make rs587779975(-;AA)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412454

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779975
dbSNP (classic)	rs587779975
ClinGen	rs587779975
ebi	rs587779975
HLI	rs587779975
Exac	rs587779975
Gnomad	rs587779975
Varsome	rs587779975
LitVar	rs587779975
Map	rs587779975
PheGenI	rs587779975
Biobank	rs587779975
1000 genomes	rs587779975
hgdp	rs587779975
ensembl	rs587779975
geneview	rs587779975
scholar	rs587779975
google	rs587779975
pharmgkb	rs587779975
gwascentral	rs587779975
openSNP	rs587779975
23andMe	rs587779975
SNPshot	rs587779975
SNPdbe	rs587779975
MSV3d	rs587779975
GWAS Ctlg	rs587779975

Max Magnitude

0

ClinVar
Risk	rs587779975(-;-)
Alt	rs587779975(-;-)
Reference	Rs587779975(AA;AA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47639593_47639594delAA
CLNSRC
CLNACC	RCV000115539.2,