rs762667660

Orientation

plus

Stabilized

plus

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

Make rs762667660(C;T)

Make rs762667660(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

15544007

Gene

CYP4F22

is a	snp
is	mentioned by
dbSNP	rs762667660
dbSNP (classic)	rs762667660
ClinGen	rs762667660
ebi	rs762667660
HLI	rs762667660
Exac	rs762667660
Gnomad	rs762667660
Varsome	rs762667660
LitVar	rs762667660
Map	rs762667660
PheGenI	rs762667660
Biobank	rs762667660
1000 genomes	rs762667660
hgdp	rs762667660
ensembl	rs762667660
geneview	rs762667660
scholar	rs762667660
google	rs762667660
pharmgkb	rs762667660
gwascentral	rs762667660
openSNP	rs762667660
23andMe	rs762667660
SNPshot	rs762667660
SNPdbe	rs762667660
MSV3d	rs762667660
GWAS Ctlg	rs762667660

Max Magnitude

0

ClinVar
Risk	rs762667660(G;G) rs762667660(T;T)
Alt	rs762667660(G;G) rs762667660(T;T)
Reference	Rs762667660(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CYP4F22
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.15654818C>T
CLNSRC
CLNACC	RCV000484186.1,