rs137854570

Orientation

plus

Stabilized

plus

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

Make rs137854570(C;G)

Make rs137854570(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

112837732

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs137854570
dbSNP (classic)	rs137854570
ClinGen	rs137854570
ebi	rs137854570
HLI	rs137854570
Exac	rs137854570
Gnomad	rs137854570
Varsome	rs137854570
LitVar	rs137854570
Map	rs137854570
PheGenI	rs137854570
Biobank	rs137854570
1000 genomes	rs137854570
hgdp	rs137854570
ensembl	rs137854570
geneview	rs137854570
scholar	rs137854570
google	rs137854570
pharmgkb	rs137854570
gwascentral	rs137854570
openSNP	rs137854570
23andMe	rs137854570
SNPshot	rs137854570
SNPdbe	rs137854570
MSV3d	rs137854570
GWAS Ctlg	rs137854570

Max Magnitude

0

OMIM	611731
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137854570(G;G)
Alt	rs137854570(G;G)
Reference	Rs137854570(C;C)
Significance	Pathogenic
Disease	Gardner syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Gardner syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112173429C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000837.5, RCV000491636.1,