rs137853865

Orientation

minus

Stabilized

minus

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

Make rs137853865(-;-)

Make rs137853865(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

64162867

Gene

PPIB

is a	snp
is	mentioned by
dbSNP	rs137853865
dbSNP (classic)	rs137853865
ClinGen	rs137853865
ebi	rs137853865
HLI	rs137853865
Exac	rs137853865
Gnomad	rs137853865
Varsome	rs137853865
LitVar	rs137853865
Map	rs137853865
PheGenI	rs137853865
Biobank	rs137853865
1000 genomes	rs137853865
hgdp	rs137853865
ensembl	rs137853865
geneview	rs137853865
scholar	rs137853865
google	rs137853865
pharmgkb	rs137853865
gwascentral	rs137853865
openSNP	rs137853865
23andMe	rs137853865
SNPshot	rs137853865
SNPdbe	rs137853865
MSV3d	rs137853865
GWAS Ctlg	rs137853865

Max Magnitude

0

ClinVar
Risk	rs137853865(-;-)
Alt	rs137853865(-;-)
Reference	Rs137853865(C;C)
Significance	Pathogenic
Disease	not provided Osteogenesis imperfecta type 9
Variation	info
Gene	PPIB
CLNDBN	not provided Osteogenesis imperfecta type 9
Reversed	1
HGVS	NC_000015.9:g.64455066delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024537.1, RCV000202411.1,