rs11254385

Orientation

plus

Stabilized

plus

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

Make rs11254385(A;A)

Make rs11254385(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

17129763

Gene

CUBN

is a	snp
is	mentioned by
dbSNP	rs11254385
dbSNP (classic)	rs11254385
ClinGen	rs11254385
ebi	rs11254385
HLI	rs11254385
Exac	rs11254385
Gnomad	rs11254385
Varsome	rs11254385
LitVar	rs11254385
Map	rs11254385
PheGenI	rs11254385
Biobank	rs11254385
1000 genomes	rs11254385
hgdp	rs11254385
ensembl	rs11254385
geneview	rs11254385
scholar	rs11254385
google	rs11254385
pharmgkb	rs11254385
gwascentral	rs11254385
openSNP	rs11254385
23andMe	rs11254385
SNPshot	rs11254385
SNPdbe	rs11254385
MSV3d	rs11254385
GWAS Ctlg	rs11254385

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

ClinVar
Risk	rs11254385(A;A)
Alt	rs11254385(A;A)
Reference	Rs11254385(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CUBN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.17171762C>A
CLNSRC
CLNACC	RCV000413849.1,