rs387906555

Orientation

plus

Stabilized

plus

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

Make rs387906555(A;A)

Make rs387906555(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

53526629

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs387906555
dbSNP (classic)	rs387906555
ClinGen	rs387906555
ebi	rs387906555
HLI	rs387906555
Exac	rs387906555
Gnomad	rs387906555
Varsome	rs387906555
LitVar	rs387906555
Map	rs387906555
PheGenI	rs387906555
Biobank	rs387906555
1000 genomes	rs387906555
hgdp	rs387906555
ensembl	rs387906555
geneview	rs387906555
scholar	rs387906555
google	rs387906555
pharmgkb	rs387906555
gwascentral	rs387906555
openSNP	rs387906555
23andMe	rs387906555
SNPshot	rs387906555
SNPdbe	rs387906555
MSV3d	rs387906555
GWAS Ctlg	rs387906555

Max Magnitude

0

ClinVar
Risk	rs387906555(A;A) rs387906555(T;T)
Alt	rs387906555(A;A) rs387906555(T;T)
Reference	Rs387906555(C;C)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	DCC
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000018.9:g.51052999C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018603.4,