rs587776701

Orientation

plus

Stabilized

plus

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

Make rs587776701(-;-)

Make rs587776701(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

80675103

Gene

MSH3

is a	snp
is	mentioned by
dbSNP	rs587776701
dbSNP (classic)	rs587776701
ClinGen	rs587776701
ebi	rs587776701
HLI	rs587776701
Exac	rs587776701
Gnomad	rs587776701
Varsome	rs587776701
LitVar	rs587776701
Map	rs587776701
PheGenI	rs587776701
Biobank	rs587776701
1000 genomes	rs587776701
hgdp	rs587776701
ensembl	rs587776701
geneview	rs587776701
scholar	rs587776701
google	rs587776701
pharmgkb	rs587776701
gwascentral	rs587776701
openSNP	rs587776701
23andMe	rs587776701
SNPshot	rs587776701
SNPdbe	rs587776701
MSV3d	rs587776701
GWAS Ctlg	rs587776701

Max Magnitude

0

ClinVar
Risk	rs587776701(-;-)
Alt	rs587776701(-;-)
Reference	Rs587776701(A;A)
Significance	Pathogenic
Disease	Familial adenomatous polyposis 4 Endometrial carcinoma
Variation	info
Gene	MSH3
CLNDBN	Familial adenomatous polyposis 4 Endometrial carcinoma
Reversed	0
HGVS	NC_000005.9:g.79970922delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009277.6, RCV000240050.1,