rs1057524581

Orientation

minus

Stabilized

minus

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

Make rs1057524581(G;T)

Make rs1057524581(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

151688291

Gene

NEB

is a	snp
is	mentioned by
dbSNP	rs1057524581
dbSNP (classic)	rs1057524581
ClinGen	rs1057524581
ebi	rs1057524581
HLI	rs1057524581
Exac	rs1057524581
Gnomad	rs1057524581
Varsome	rs1057524581
LitVar	rs1057524581
Map	rs1057524581
PheGenI	rs1057524581
Biobank	rs1057524581
1000 genomes	rs1057524581
hgdp	rs1057524581
ensembl	rs1057524581
geneview	rs1057524581
scholar	rs1057524581
google	rs1057524581
pharmgkb	rs1057524581
gwascentral	rs1057524581
openSNP	rs1057524581
23andMe	rs1057524581
SNPshot	rs1057524581
SNPdbe	rs1057524581
MSV3d	rs1057524581
GWAS Ctlg	rs1057524581

Max Magnitude

0

ClinVar
Risk	rs1057524581(A;A) rs1057524581(T;T)
Alt	rs1057524581(A;A) rs1057524581(T;T)
Reference	Rs1057524581(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NEB
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.152544805C>A; NC_000002.11:g.152544805C>T
CLNSRC
CLNACC	RCV000437465.1, RCV000487268.1,