rs104893626

Orientation

minus

Stabilized

minus

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

Make rs104893626(C;G)

Make rs104893626(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

136114915

Gene

CXCR4

is a	snp
is	mentioned by
dbSNP	rs104893626
dbSNP (classic)	rs104893626
ClinGen	rs104893626
ebi	rs104893626
HLI	rs104893626
Exac	rs104893626
Gnomad	rs104893626
Varsome	rs104893626
LitVar	rs104893626
Map	rs104893626
PheGenI	rs104893626
Biobank	rs104893626
1000 genomes	rs104893626
hgdp	rs104893626
ensembl	rs104893626
geneview	rs104893626
scholar	rs104893626
google	rs104893626
pharmgkb	rs104893626
gwascentral	rs104893626
openSNP	rs104893626
23andMe	rs104893626
SNPshot	rs104893626
SNPdbe	rs104893626
MSV3d	rs104893626
GWAS Ctlg	rs104893626

Max Magnitude

0

OMIM	162643
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104893626(G;G)
Alt	rs104893626(G;G)
Reference	Rs104893626(C;C)
Significance	Pathogenic
Disease	Warts
Variation	info
Gene	CXCR4
CLNDBN	Warts, hypogammaglobulinemia, infections, and myelokathexis
Reversed	1
HGVS	NC_000002.11:g.136872485G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015067.26,