rs606231474

Orientation

minus

Stabilized

minus

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

Make rs606231474(-;-)

Make rs606231474(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

36471473

Gene

CSF3R

is a	snp
is	mentioned by
dbSNP	rs606231474
dbSNP (classic)	rs606231474
ClinGen	rs606231474
ebi	rs606231474
HLI	rs606231474
Exac	rs606231474
Gnomad	rs606231474
Varsome	rs606231474
LitVar	rs606231474
Map	rs606231474
PheGenI	rs606231474
Biobank	rs606231474
1000 genomes	rs606231474
hgdp	rs606231474
ensembl	rs606231474
geneview	rs606231474
scholar	rs606231474
google	rs606231474
pharmgkb	rs606231474
gwascentral	rs606231474
openSNP	rs606231474
23andMe	rs606231474
SNPshot	rs606231474
SNPdbe	rs606231474
MSV3d	rs606231474
GWAS Ctlg	rs606231474

Max Magnitude

0

ClinVar
Risk	rs606231474(-;-)
Alt	rs606231474(-;-)
Reference	Rs606231474(G;G)
Significance	Pathogenic
Disease	Severe congenital neutropenia Neutropenia
Variation	info
Gene	CSF3R
CLNDBN	Severe congenital neutropenia Neutropenia, severe congenital, 7, autosomal recessive
Reversed	1
HGVS	NC_000001.10:g.36937074delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149409.1, RCV000234853.1,