rs773009397

Orientation

plus

Stabilized

plus

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

Make rs773009397(A;A)

Make rs773009397(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

40397178

Gene

PRX

is a	snp
is	mentioned by
dbSNP	rs773009397
dbSNP (classic)	rs773009397
ClinGen	rs773009397
ebi	rs773009397
HLI	rs773009397
Exac	rs773009397
Gnomad	rs773009397
Varsome	rs773009397
LitVar	rs773009397
Map	rs773009397
PheGenI	rs773009397
Biobank	rs773009397
1000 genomes	rs773009397
hgdp	rs773009397
ensembl	rs773009397
geneview	rs773009397
scholar	rs773009397
google	rs773009397
pharmgkb	rs773009397
gwascentral	rs773009397
openSNP	rs773009397
23andMe	rs773009397
SNPshot	rs773009397
SNPdbe	rs773009397
MSV3d	rs773009397
GWAS Ctlg	rs773009397

Max Magnitude

0

ClinVar
Risk	rs773009397(A;A)
Alt	rs773009397(A;A)
Reference	Rs773009397(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PRX
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.40903085G>A
CLNSRC
CLNACC	RCV000235669.1,