rs387906400

Orientation

minus

Stabilized

minus

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

Make rs387906400(A;A)

Make rs387906400(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

44378102

Gene

CXCL12

is a	snp
is	mentioned by
dbSNP	rs387906400
dbSNP (classic)	rs387906400
ClinGen	rs387906400
ebi	rs387906400
HLI	rs387906400
Exac	rs387906400
Gnomad	rs387906400
Varsome	rs387906400
LitVar	rs387906400
Map	rs387906400
PheGenI	rs387906400
Biobank	rs387906400
1000 genomes	rs387906400
hgdp	rs387906400
ensembl	rs387906400
geneview	rs387906400
scholar	rs387906400
google	rs387906400
pharmgkb	rs387906400
gwascentral	rs387906400
openSNP	rs387906400
23andMe	rs387906400
SNPshot	rs387906400
SNPdbe	rs387906400
MSV3d	rs387906400
GWAS Ctlg	rs387906400

Max Magnitude

0

ClinVar
Risk	rs387906400(A;A)
Alt	rs387906400(A;A)
Reference	Rs387906400(G;G)
Significance	Other
Disease	Human immunodeficiency virus type 1
Variation	info
Gene	CXCL12
CLNDBN	Human immunodeficiency virus type 1, susceptibility to
Reversed	1
HGVS	NC_000010.10:g.44873550C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009307.3,