rs1057518087

Orientation

plus

Stabilized

plus

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

Make rs1057518087(C;G)

Make rs1057518087(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

15529699

Gene

CYP4F22

is a	snp
is	mentioned by
dbSNP	rs1057518087
dbSNP (classic)	rs1057518087
ClinGen	rs1057518087
ebi	rs1057518087
HLI	rs1057518087
Exac	rs1057518087
Gnomad	rs1057518087
Varsome	rs1057518087
LitVar	rs1057518087
Map	rs1057518087
PheGenI	rs1057518087
Biobank	rs1057518087
1000 genomes	rs1057518087
hgdp	rs1057518087
ensembl	rs1057518087
geneview	rs1057518087
scholar	rs1057518087
google	rs1057518087
pharmgkb	rs1057518087
gwascentral	rs1057518087
openSNP	rs1057518087
23andMe	rs1057518087
SNPshot	rs1057518087
SNPdbe	rs1057518087
MSV3d	rs1057518087
GWAS Ctlg	rs1057518087

Max Magnitude

0

ClinVar
Risk	rs1057518087(G;G)
Alt	rs1057518087(G;G)
Reference	Rs1057518087(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CYP4F22
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.15640510C>G
CLNSRC
CLNACC	RCV000414461.1,