rs137852338

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(ATC;ATC)	0	common/normal
(TCA;TCA)	0	common in clinvar

Make rs137852338(-;-)

Make rs137852338(-;ATC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154546051

Gene	G6PD, IKBKG

is a	snp
is	mentioned by
dbSNP	rs137852338
dbSNP (classic)	rs137852338
ClinGen	rs137852338
ebi	rs137852338
HLI	rs137852338
Exac	rs137852338
Gnomad	rs137852338
Varsome	rs137852338
LitVar	rs137852338
Map	rs137852338
PheGenI	rs137852338
Biobank	rs137852338
1000 genomes	rs137852338
hgdp	rs137852338
ensembl	rs137852338
geneview	rs137852338
scholar	rs137852338
google	rs137852338
pharmgkb	rs137852338
gwascentral	rs137852338
openSNP	rs137852338
23andMe	rs137852338
SNPshot	rs137852338
SNPdbe	rs137852338
MSV3d	rs137852338
GWAS Ctlg	rs137852338

Max Magnitude

0

OMIM	305900
Desc
Variant	0041
Related	also

ClinVar
Risk	rs137852338(-;-)
Alt	rs137852338(-;-)
Reference	rs137852338(CAT;CAT)
Significance	Other
Disease	G6PD SUNDERLAND Anemia
Variation	info
Gene	IKBKG G6PD
CLNDBN	G6PD SUNDERLAND Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed	1
HGVS	NC_000023.10:g.153774266_153774268delGAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011140.2, RCV000011141.3,