rs387907356

Orientation

plus

Stabilized

plus

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

Make rs387907356(A;A)

Make rs387907356(A;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

48981411

Gene

WNT1

is a	snp
is	mentioned by
dbSNP	rs387907356
dbSNP (classic)	rs387907356
ClinGen	rs387907356
ebi	rs387907356
HLI	rs387907356
Exac	rs387907356
Gnomad	rs387907356
Varsome	rs387907356
LitVar	rs387907356
Map	rs387907356
PheGenI	rs387907356
Biobank	rs387907356
1000 genomes	rs387907356
hgdp	rs387907356
ensembl	rs387907356
geneview	rs387907356
scholar	rs387907356
google	rs387907356
pharmgkb	rs387907356
gwascentral	rs387907356
openSNP	rs387907356
23andMe	rs387907356
SNPshot	rs387907356
SNPdbe	rs387907356
MSV3d	rs387907356
GWAS Ctlg	rs387907356

Max Magnitude

0

ClinVar
Risk	rs387907356(A;A)
Alt	rs387907356(A;A)
Reference	Rs387907356(C;C)
Significance	Pathogenic
Disease	Osteogenesis imperfecta not provided
Variation	info
Gene	WNT1
CLNDBN	Osteogenesis imperfecta, type xv not provided
Reversed	0
HGVS	NC_000012.11:g.49375194C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043495.30, RCV000489304.1,