rs886037879

Orientation

plus

Stabilized

plus

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

Make rs886037879(-;-)

Make rs886037879(-;C)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

80813688

Gene

MSH3

is a	snp
is	mentioned by
dbSNP	rs886037879
dbSNP (classic)	rs886037879
ClinGen	rs886037879
ebi	rs886037879
HLI	rs886037879
Exac	rs886037879
Gnomad	rs886037879
Varsome	rs886037879
LitVar	rs886037879
Map	rs886037879
PheGenI	rs886037879
Biobank	rs886037879
1000 genomes	rs886037879
hgdp	rs886037879
ensembl	rs886037879
geneview	rs886037879
scholar	rs886037879
google	rs886037879
pharmgkb	rs886037879
gwascentral	rs886037879
openSNP	rs886037879
23andMe	rs886037879
SNPshot	rs886037879
SNPdbe	rs886037879
MSV3d	rs886037879
GWAS Ctlg	rs886037879

Max Magnitude

0

ClinVar
Risk	rs886037879(-;-)
Alt	rs886037879(-;-)
Reference	Rs886037879(C;C)
Significance	Pathogenic
Disease	Familial adenomatous polyposis 4
Variation	info
Gene	MSH3
CLNDBN	Familial adenomatous polyposis 4
Reversed	0
HGVS	NC_000005.9:g.80109507delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000240520.1,