rs1800940

Orientation

plus

Stabilized

plus

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

Make rs1800940(G;T)

Make rs1800940(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

46373082

Gene	CCR5, LOC102724297

is a	snp
is	mentioned by
dbSNP	rs1800940
dbSNP (classic)	rs1800940
ClinGen	rs1800940
ebi	rs1800940
HLI	rs1800940
Exac	rs1800940
Gnomad	rs1800940
Varsome	rs1800940
LitVar	rs1800940
Map	rs1800940
PheGenI	rs1800940
Biobank	rs1800940
1000 genomes	rs1800940
hgdp	rs1800940
ensembl	rs1800940
geneview	rs1800940
scholar	rs1800940
google	rs1800940
pharmgkb	rs1800940
gwascentral	rs1800940
openSNP	rs1800940
23andMe	rs1800940
SNPshot	rs1800940
SNPdbe	rs1800940
MSV3d	rs1800940
GWAS Ctlg	rs1800940

Max Magnitude

0

OMIM	601373
Desc
Variant	0008
Related	also

ClinVar
Risk	rs1800940(T;T)
Alt	rs1800940(T;T)
Reference	Rs1800940(G;G)
Significance	Other
Disease	Human immunodeficiency virus type 1
Variation	info
Gene	LOC102724297 CCR5
CLNDBN	Human immunodeficiency virus type 1, susceptibility to
Reversed	0
HGVS	NC_000003.11:g.46414573G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008673.4,