rs74315310

Orientation

plus

Stabilized

plus

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

Make rs74315310(C;T)

Make rs74315310(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

149784224

Gene	FCGR1A, HIST2H2BF

is a	snp
is	mentioned by
dbSNP	rs74315310
dbSNP (classic)	rs74315310
ClinGen	rs74315310
ebi	rs74315310
HLI	rs74315310
Exac	rs74315310
Gnomad	rs74315310
Varsome	rs74315310
LitVar	rs74315310
Map	rs74315310
PheGenI	rs74315310
Biobank	rs74315310
1000 genomes	rs74315310
hgdp	rs74315310
ensembl	rs74315310
geneview	rs74315310
scholar	rs74315310
google	rs74315310
pharmgkb	rs74315310
gwascentral	rs74315310
openSNP	rs74315310
23andMe	rs74315310
SNPshot	rs74315310
SNPdbe	rs74315310
MSV3d	rs74315310
GWAS Ctlg	rs74315310

Max Magnitude

0

OMIM	146760
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315310(T;T)
Alt	rs74315310(T;T)
Reference	Rs74315310(C;C)
Significance	Pathogenic
Disease	IGG receptor I
Variation	info
Gene	FCGR1A HIST2H2BF
CLNDBN	IGG receptor I, phagocytic, familial deficiency of
Reversed	0
HGVS	NC_000001.10:g.149755780C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015950.26,