rs1057516045

Orientation

minus

Stabilized

minus

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

Make rs1057516045(C;T)

Make rs1057516045(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

225403404

Gene

LBR

is a	snp
is	mentioned by
dbSNP	rs1057516045
dbSNP (classic)	rs1057516045
ClinGen	rs1057516045
ebi	rs1057516045
HLI	rs1057516045
Exac	rs1057516045
Gnomad	rs1057516045
Varsome	rs1057516045
LitVar	rs1057516045
Map	rs1057516045
PheGenI	rs1057516045
Biobank	rs1057516045
1000 genomes	rs1057516045
hgdp	rs1057516045
ensembl	rs1057516045
geneview	rs1057516045
scholar	rs1057516045
google	rs1057516045
pharmgkb	rs1057516045
gwascentral	rs1057516045
openSNP	rs1057516045
23andMe	rs1057516045
SNPshot	rs1057516045
SNPdbe	rs1057516045
MSV3d	rs1057516045
GWAS Ctlg	rs1057516045

Max Magnitude

0

ClinVar
Risk	rs1057516045(T;T)
Alt	rs1057516045(T;T)
Reference	Rs1057516045(C;C)
Significance	Probable-Pathogenic
Disease	Pelger-Huët anomaly
Variation	info
Gene	LBR
CLNDBN	Pelger-Huët anomaly
Reversed	1
HGVS	NC_000001.10:g.225591106G>A
CLNSRC
CLNACC	RCV000408612.1,