rs74315322

Orientation

plus

Stabilized

plus

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

Make rs74315322(C;T)

Make rs74315322(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154275165

Gene

HAX1

is a	snp
is	mentioned by
dbSNP	rs74315322
dbSNP (classic)	rs74315322
ClinGen	rs74315322
ebi	rs74315322
HLI	rs74315322
Exac	rs74315322
Gnomad	rs74315322
Varsome	rs74315322
LitVar	rs74315322
Map	rs74315322
PheGenI	rs74315322
Biobank	rs74315322
1000 genomes	rs74315322
hgdp	rs74315322
ensembl	rs74315322
geneview	rs74315322
scholar	rs74315322
google	rs74315322
pharmgkb	rs74315322
gwascentral	rs74315322
openSNP	rs74315322
23andMe	rs74315322
SNPshot	rs74315322
SNPdbe	rs74315322
MSV3d	rs74315322
GWAS Ctlg	rs74315322

Max Magnitude

0

OMIM	605998
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315322(T;T)
Alt	rs74315322(T;T)
Reference	Rs74315322(C;C)
Significance	Pathogenic
Disease	Severe congenital neutropenia 3
Variation	info
Gene	HAX1
CLNDBN	Severe congenital neutropenia 3, autosomal recessive
Reversed	0
HGVS	NC_000001.10:g.154247641C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004913.2,