rs137853322

Orientation

plus

Stabilized

plus

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

Make rs137853322(A;G)

Make rs137853322(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154564420

Gene

IKBKG

is a	snp
is	mentioned by
dbSNP	rs137853322
dbSNP (classic)	rs137853322
ClinGen	rs137853322
ebi	rs137853322
HLI	rs137853322
Exac	rs137853322
Gnomad	rs137853322
Varsome	rs137853322
LitVar	rs137853322
Map	rs137853322
PheGenI	rs137853322
Biobank	rs137853322
1000 genomes	rs137853322
hgdp	rs137853322
ensembl	rs137853322
geneview	rs137853322
scholar	rs137853322
google	rs137853322
pharmgkb	rs137853322
gwascentral	rs137853322
openSNP	rs137853322
23andMe	rs137853322
SNPshot	rs137853322
SNPdbe	rs137853322
MSV3d	rs137853322
GWAS Ctlg	rs137853322

Max Magnitude

0

OMIM	300248
Desc
Variant	0005
Related	also

ClinVar
Risk	rs137853322(G;G)
Alt	rs137853322(G;G)
Reference	Rs137853322(A;A)
Significance	Pathogenic
Disease	Incontinentia pigmenti syndrome
Variation	info
Gene	IKBKG
CLNDBN	Incontinentia pigmenti syndrome
Reversed	0
HGVS	NC_000023.10:g.153792635A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012202.3,