rs5030878

Orientation

minus

Stabilized

minus

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

Make rs5030878(C;C)

Make rs5030878(C;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

51746963

Gene

FPR1

is a	snp
is	mentioned by
dbSNP	rs5030878
dbSNP (classic)	rs5030878
ClinGen	rs5030878
ebi	rs5030878
HLI	rs5030878
Exac	rs5030878
Gnomad	rs5030878
Varsome	rs5030878
LitVar	rs5030878
Map	rs5030878
PheGenI	rs5030878
Biobank	rs5030878
1000 genomes	rs5030878
hgdp	rs5030878
ensembl	rs5030878
geneview	rs5030878
scholar	rs5030878
google	rs5030878
pharmgkb	rs5030878
gwascentral	rs5030878
openSNP	rs5030878
23andMe	rs5030878
SNPshot	rs5030878
SNPdbe	rs5030878
MSV3d	rs5030878
GWAS Ctlg	rs5030878

GMAF

0.1736

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 21144844] Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels.

[PMID 23373827] V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins.

ClinVar
Risk	rs5030878(C;C)
Alt	rs5030878(C;C)
Reference	Rs5030878(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	FPR1
CLNDBN	not specified
Reversed	1
HGVS	NC_000019.9:g.52250216A>G
CLNSRC
CLNACC	RCV000455423.1,