rs886037878

Orientation

plus

Stabilized

plus

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

Make rs886037878(A;C)

Make rs886037878(C;C)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

80864811

Gene

MSH3

is a	snp
is	mentioned by
dbSNP	rs886037878
dbSNP (classic)	rs886037878
ClinGen	rs886037878
ebi	rs886037878
HLI	rs886037878
Exac	rs886037878
Gnomad	rs886037878
Varsome	rs886037878
LitVar	rs886037878
Map	rs886037878
PheGenI	rs886037878
Biobank	rs886037878
1000 genomes	rs886037878
hgdp	rs886037878
ensembl	rs886037878
geneview	rs886037878
scholar	rs886037878
google	rs886037878
pharmgkb	rs886037878
gwascentral	rs886037878
openSNP	rs886037878
23andMe	rs886037878
SNPshot	rs886037878
SNPdbe	rs886037878
MSV3d	rs886037878
GWAS Ctlg	rs886037878

Max Magnitude

0

ClinVar
Risk	rs886037878(C;C)
Alt	rs886037878(C;C)
Reference	Rs886037878(A;A)
Significance	Pathogenic
Disease	Familial adenomatous polyposis 4
Variation	info
Gene	MSH3
CLNDBN	Familial adenomatous polyposis 4
Reversed	0
HGVS	NC_000005.9:g.80160630A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000240222.1,