rs1057517778

Orientation

minus

Stabilized

minus

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

Make rs1057517778(-;-)

Make rs1057517778(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

30308784

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs1057517778
dbSNP (classic)	rs1057517778
ClinGen	rs1057517778
ebi	rs1057517778
HLI	rs1057517778
Exac	rs1057517778
Gnomad	rs1057517778
Varsome	rs1057517778
LitVar	rs1057517778
Map	rs1057517778
PheGenI	rs1057517778
Biobank	rs1057517778
1000 genomes	rs1057517778
hgdp	rs1057517778
ensembl	rs1057517778
geneview	rs1057517778
scholar	rs1057517778
google	rs1057517778
pharmgkb	rs1057517778
gwascentral	rs1057517778
openSNP	rs1057517778
23andMe	rs1057517778
SNPshot	rs1057517778
SNPdbe	rs1057517778
MSV3d	rs1057517778
GWAS Ctlg	rs1057517778

Max Magnitude

0

ClinVar
Risk	rs1057517778(-;-)
Alt	rs1057517778(-;-)
Reference	Rs1057517778(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NR0B1
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.30326901delC
CLNSRC
CLNACC	RCV000413027.1,