rs730881227

Orientation

plus

Stabilized

plus

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

Make rs730881227(A;A)

Make rs730881227(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112779849

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs730881227
dbSNP (classic)	rs730881227
ClinGen	rs730881227
ebi	rs730881227
HLI	rs730881227
Exac	rs730881227
Gnomad	rs730881227
Varsome	rs730881227
LitVar	rs730881227
Map	rs730881227
PheGenI	rs730881227
Biobank	rs730881227
1000 genomes	rs730881227
hgdp	rs730881227
ensembl	rs730881227
geneview	rs730881227
scholar	rs730881227
google	rs730881227
pharmgkb	rs730881227
gwascentral	rs730881227
openSNP	rs730881227
23andMe	rs730881227
SNPshot	rs730881227
SNPdbe	rs730881227
MSV3d	rs730881227
GWAS Ctlg	rs730881227

Max Magnitude

0

ClinVar
Risk	rs730881227(A;A)
Alt	rs730881227(A;A)
Reference	Rs730881227(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112115546G>A
CLNSRC
CLNACC	RCV000159516.1,