rs147214773

Orientation

plus

Stabilized

plus

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

Make rs147214773(C;T)

Make rs147214773(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

136114925

Gene

CXCR4

is a	snp
is	mentioned by
dbSNP	rs147214773
dbSNP (classic)	rs147214773
ClinGen	rs147214773
ebi	rs147214773
HLI	rs147214773
Exac	rs147214773
Gnomad	rs147214773
Varsome	rs147214773
LitVar	rs147214773
Map	rs147214773
PheGenI	rs147214773
Biobank	rs147214773
1000 genomes	rs147214773
hgdp	rs147214773
ensembl	rs147214773
geneview	rs147214773
scholar	rs147214773
google	rs147214773
pharmgkb	rs147214773
gwascentral	rs147214773
openSNP	rs147214773
23andMe	rs147214773
SNPshot	rs147214773
SNPdbe	rs147214773
MSV3d	rs147214773
GWAS Ctlg	rs147214773

Max Magnitude

0

ClinVar
Risk	rs147214773(T;T)
Alt	rs147214773(T;T)
Reference	Rs147214773(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CXCR4
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.136872495C>T
CLNSRC
CLNACC	RCV000413464.1,