rs137853869

Orientation

minus

Stabilized

minus

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

Make rs137853869(-;-)

Make rs137853869(-;AAGA)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

64156115

Gene	PPIB, SNX22

is a	snp
is	mentioned by
dbSNP	rs137853869
dbSNP (classic)	rs137853869
ClinGen	rs137853869
ebi	rs137853869
HLI	rs137853869
Exac	rs137853869
Gnomad	rs137853869
Varsome	rs137853869
LitVar	rs137853869
Map	rs137853869
PheGenI	rs137853869
Biobank	rs137853869
1000 genomes	rs137853869
hgdp	rs137853869
ensembl	rs137853869
geneview	rs137853869
scholar	rs137853869
google	rs137853869
pharmgkb	rs137853869
gwascentral	rs137853869
openSNP	rs137853869
23andMe	rs137853869
SNPshot	rs137853869
SNPdbe	rs137853869
MSV3d	rs137853869
GWAS Ctlg	rs137853869

Max Magnitude

0

ClinVar
Risk	rs137853869(-;-)
Alt	rs137853869(-;-)
Reference	Rs137853869(AAGA;AAGA)
Significance	Pathogenic
Disease	Osteogenesis imperfecta type 9 not provided
Variation	info
Gene	PPIB SNX22
CLNDBN	Osteogenesis imperfecta type 9 not provided
Reversed	1
HGVS	NC_000015.9:g.64448314_64448317delTCTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018433.27, RCV000024535.1,