rs132630275

Orientation

plus

Stabilized

plus

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

Make rs132630275(C;G)

Make rs132630275(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

48684323

Gene

WAS

is a	snp
is	mentioned by
dbSNP	rs132630275
dbSNP (classic)	rs132630275
ClinGen	rs132630275
ebi	rs132630275
HLI	rs132630275
Exac	rs132630275
Gnomad	rs132630275
Varsome	rs132630275
LitVar	rs132630275
Map	rs132630275
PheGenI	rs132630275
Biobank	rs132630275
1000 genomes	rs132630275
hgdp	rs132630275
ensembl	rs132630275
geneview	rs132630275
scholar	rs132630275
google	rs132630275
pharmgkb	rs132630275
gwascentral	rs132630275
openSNP	rs132630275
23andMe	rs132630275
SNPshot	rs132630275
SNPdbe	rs132630275
MSV3d	rs132630275
GWAS Ctlg	rs132630275

Merged from

Rs28935178

Max Magnitude

0

OMIM	300392
Desc
Variant	0013
Related	also

ClinVar
Risk	rs132630275(A;A) rs132630275(G;G)
Alt	rs132630275(A;A) rs132630275(G;G)
Reference	Rs132630275(C;C)
Significance	Pathogenic
Disease	not provided Thrombocytopenia
Variation	info
Gene	WAS
CLNDBN	not provided Thrombocytopenia, X-linked, intermittent
Reversed	0
HGVS	NC_000023.10:g.48542712C>A; NC_000023.10:g.48542712C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000485571.1, RCV000011875.7,