rs866260675

Orientation

plus

Stabilized

plus

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

Make rs866260675(A;A)

Make rs866260675(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

80778719

Gene

MSH3

is a	snp
is	mentioned by
dbSNP	rs866260675
dbSNP (classic)	rs866260675
ClinGen	rs866260675
ebi	rs866260675
HLI	rs866260675
Exac	rs866260675
Gnomad	rs866260675
Varsome	rs866260675
LitVar	rs866260675
Map	rs866260675
PheGenI	rs866260675
Biobank	rs866260675
1000 genomes	rs866260675
hgdp	rs866260675
ensembl	rs866260675
geneview	rs866260675
scholar	rs866260675
google	rs866260675
pharmgkb	rs866260675
gwascentral	rs866260675
openSNP	rs866260675
23andMe	rs866260675
SNPshot	rs866260675
SNPdbe	rs866260675
MSV3d	rs866260675
GWAS Ctlg	rs866260675

Max Magnitude

0

ClinVar
Risk	rs866260675(A;A)
Alt	rs866260675(A;A)
Reference	Rs866260675(G;G)
Significance	Pathogenic
Disease	Familial adenomatous polyposis 4
Variation	info
Gene	MSH3
CLNDBN	Familial adenomatous polyposis 4
Reversed	0
HGVS	NC_000005.9:g.80074538G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000240037.1,