rs132630268

Orientation

plus

Stabilized

plus

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

Make rs132630268(G;T)

Make rs132630268(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

48684407

Gene

WAS

is a	snp
is	mentioned by
dbSNP	rs132630268
dbSNP (classic)	rs132630268
ClinGen	rs132630268
ebi	rs132630268
HLI	rs132630268
Exac	rs132630268
Gnomad	rs132630268
Varsome	rs132630268
LitVar	rs132630268
Map	rs132630268
PheGenI	rs132630268
Biobank	rs132630268
1000 genomes	rs132630268
hgdp	rs132630268
ensembl	rs132630268
geneview	rs132630268
scholar	rs132630268
google	rs132630268
pharmgkb	rs132630268
gwascentral	rs132630268
openSNP	rs132630268
23andMe	rs132630268
SNPshot	rs132630268
SNPdbe	rs132630268
MSV3d	rs132630268
GWAS Ctlg	rs132630268

Max Magnitude

0

OMIM	300392
Desc
Variant	0002
Related	also

OMIM	300392
Desc
Variant	0003
Related	also

ClinVar
Risk	rs132630268(A;A) rs132630268(T;T)
Alt	rs132630268(A;A) rs132630268(T;T)
Reference	Rs132630268(G;G)
Significance	Pathogenic
Disease	Wiskott-Aldrich syndrome not provided
Variation	info
Gene	WAS
CLNDBN	Wiskott-Aldrich syndrome not provided
Reversed	0
HGVS	NC_000023.10:g.48542796G>A; NC_000023.10:g.48542796G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011864.6, RCV000414284.1, RCV000011863.18,