rs869312934

Orientation

minus

Stabilized

minus

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

Make rs869312934(C;T)

Make rs869312934(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

160279842

Gene

PEX19

is a	snp
is	mentioned by
dbSNP	rs869312934
dbSNP (classic)	rs869312934
ClinGen	rs869312934
ebi	rs869312934
HLI	rs869312934
Exac	rs869312934
Gnomad	rs869312934
Varsome	rs869312934
LitVar	rs869312934
Map	rs869312934
PheGenI	rs869312934
Biobank	rs869312934
1000 genomes	rs869312934
hgdp	rs869312934
ensembl	rs869312934
geneview	rs869312934
scholar	rs869312934
google	rs869312934
pharmgkb	rs869312934
gwascentral	rs869312934
openSNP	rs869312934
23andMe	rs869312934
SNPshot	rs869312934
SNPdbe	rs869312934
MSV3d	rs869312934
GWAS Ctlg	rs869312934

Max Magnitude

0

ClinVar
Risk	rs869312934(T;T)
Alt	rs869312934(T;T)
Reference	Rs869312934(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	PEX19
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000001.10:g.160249632G>A
CLNSRC
CLNACC	RCV000210599.1,