rs137854571

Orientation

plus

Stabilized

plus

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

Make rs137854571(C;T)

Make rs137854571(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

112838793

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs137854571
dbSNP (classic)	rs137854571
ClinGen	rs137854571
ebi	rs137854571
HLI	rs137854571
Exac	rs137854571
Gnomad	rs137854571
Varsome	rs137854571
LitVar	rs137854571
Map	rs137854571
PheGenI	rs137854571
Biobank	rs137854571
1000 genomes	rs137854571
hgdp	rs137854571
ensembl	rs137854571
geneview	rs137854571
scholar	rs137854571
google	rs137854571
pharmgkb	rs137854571
gwascentral	rs137854571
openSNP	rs137854571
23andMe	rs137854571
SNPshot	rs137854571
SNPdbe	rs137854571
MSV3d	rs137854571
GWAS Ctlg	rs137854571

Max Magnitude

0

OMIM	611731
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137854571(T;T)
Alt	rs137854571(T;T)
Reference	Rs137854571(C;C)
Significance	Pathogenic
Disease	Neoplasm of stomach
Variation	info
Gene	APC
CLNDBN	Neoplasm of stomach
Reversed	0
HGVS	NC_000005.9:g.112174490C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000840.4,