rs1057520700

Orientation

plus

Stabilized

plus

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

Make rs1057520700(G;T)

Make rs1057520700(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

48685634

Gene

WAS

is a	snp
is	mentioned by
dbSNP	rs1057520700
dbSNP (classic)	rs1057520700
ClinGen	rs1057520700
ebi	rs1057520700
HLI	rs1057520700
Exac	rs1057520700
Gnomad	rs1057520700
Varsome	rs1057520700
LitVar	rs1057520700
Map	rs1057520700
PheGenI	rs1057520700
Biobank	rs1057520700
1000 genomes	rs1057520700
hgdp	rs1057520700
ensembl	rs1057520700
geneview	rs1057520700
scholar	rs1057520700
google	rs1057520700
pharmgkb	rs1057520700
gwascentral	rs1057520700
openSNP	rs1057520700
23andMe	rs1057520700
SNPshot	rs1057520700
SNPdbe	rs1057520700
MSV3d	rs1057520700
GWAS Ctlg	rs1057520700

Max Magnitude

0

ClinVar
Risk	rs1057520700(A;A) rs1057520700(T;T)
Alt	rs1057520700(A;A) rs1057520700(T;T)
Reference	Rs1057520700(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	WAS
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.48544023G>A; NC_000023.10:g.48544023G>T
CLNSRC
CLNACC	RCV000440734.1, RCV000426711.1,