rs104893625

Orientation

minus

Stabilized

minus

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

Make rs104893625(G;T)

Make rs104893625(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

136114901

Gene

CXCR4

is a	snp
is	mentioned by
dbSNP	rs104893625
dbSNP (classic)	rs104893625
ClinGen	rs104893625
ebi	rs104893625
HLI	rs104893625
Exac	rs104893625
Gnomad	rs104893625
Varsome	rs104893625
LitVar	rs104893625
Map	rs104893625
PheGenI	rs104893625
Biobank	rs104893625
1000 genomes	rs104893625
hgdp	rs104893625
ensembl	rs104893625
geneview	rs104893625
scholar	rs104893625
google	rs104893625
pharmgkb	rs104893625
gwascentral	rs104893625
openSNP	rs104893625
23andMe	rs104893625
SNPshot	rs104893625
SNPdbe	rs104893625
MSV3d	rs104893625
GWAS Ctlg	rs104893625

Max Magnitude

0

OMIM	162643
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893625(T;T)
Alt	rs104893625(T;T)
Reference	Rs104893625(G;G)
Significance	Pathogenic
Disease	Warts
Variation	info
Gene	CXCR4
CLNDBN	Warts, hypogammaglobulinemia, infections, and myelokathexis
Reversed	1
HGVS	NC_000002.11:g.136872471C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015066.26,