rs41469351

Orientation

plus

Stabilized

plus

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

Make rs41469351(C;T)

Make rs41469351(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46370771

Gene	CCR5, LOC102724297

is a	snp
is	mentioned by
dbSNP	rs41469351
dbSNP (classic)	rs41469351
ClinGen	rs41469351
ebi	rs41469351
HLI	rs41469351
Exac	rs41469351
Gnomad	rs41469351
Varsome	rs41469351
LitVar	rs41469351
Map	rs41469351
PheGenI	rs41469351
Biobank	rs41469351
1000 genomes	rs41469351
hgdp	rs41469351
ensembl	rs41469351
geneview	rs41469351
scholar	rs41469351
google	rs41469351
pharmgkb	rs41469351
gwascentral	rs41469351
openSNP	rs41469351
23andMe	rs41469351
SNPshot	rs41469351
SNPdbe	rs41469351
MSV3d	rs41469351
GWAS Ctlg	rs41469351

Max Magnitude

0

ClinVar
Risk	rs41469351(T;T)
Alt	rs41469351(T;T)
Reference	Rs41469351(C;C)
Significance	Pathogenic
Disease	Human immunodeficiency virus type 1
Variation	info
Gene	LOC102724297 CCR5
CLNDBN	Human immunodeficiency virus type 1, increased perinatal transmission of
Reversed	0
HGVS	NC_000003.11:g.46412262C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008672.3,