rs1042229

Orientation

minus

Stabilized

minus

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

Make rs1042229(G;G)

Make rs1042229(G;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

51746419

Gene

FPR1

is a	snp
is	mentioned by
dbSNP	rs1042229
dbSNP (classic)	rs1042229
ClinGen	rs1042229
ebi	rs1042229
HLI	rs1042229
Exac	rs1042229
Gnomad	rs1042229
Varsome	rs1042229
LitVar	rs1042229
Map	rs1042229
PheGenI	rs1042229
Biobank	rs1042229
1000 genomes	rs1042229
hgdp	rs1042229
ensembl	rs1042229
geneview	rs1042229
scholar	rs1042229
google	rs1042229
pharmgkb	rs1042229
gwascentral	rs1042229
openSNP	rs1042229
23andMe	rs1042229
SNPshot	rs1042229
SNPdbe	rs1042229
MSV3d	rs1042229
GWAS Ctlg	rs1042229

GMAF

0.4022

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

[PMID 21216225] Polymorphisms of the formylpeptide receptor gene (FPR1) and susceptibility to stomach cancer in 1,531 consecutive autopsy cases

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

ClinVar
Risk	rs1042229(C;C) rs1042229(G;G)
Alt	rs1042229(C;C) rs1042229(G;G)
Reference	Rs1042229(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	FPR1
CLNDBN	not specified
Reversed	1
HGVS	NC_000019.9:g.52249672A>C
CLNSRC
CLNACC	RCV000455271.1,