Have questions? Visit https://www.reddit.com/r/SNPedia

rs74315310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315310(C;T)
Make rs74315310(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position149784224
GeneFCGR1A, HIST2H2BF
is asnp
is mentioned by
dbSNPrs74315310
ebirs74315310
HLIrs74315310
Exacrs74315310
Varsomers74315310
Maprs74315310
PheGenIrs74315310
hapmaprs74315310
1000 genomesrs74315310
hgdprs74315310
ensemblrs74315310
gopubmedrs74315310
geneviewrs74315310
scholarrs74315310
googlers74315310
pharmgkbrs74315310
gwascentralrs74315310
openSNPrs74315310
23andMers74315310
23andMe allrs74315310
SNP Nexus

SNPshotrs74315310
SNPdbers74315310
MSV3drs74315310
GWAS Ctlgrs74315310
Max Magnitude0
OMIM146760
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315310(T;T)
Alt rs74315310(T;T)
Reference rs74315310(C;C)
Significance Pathogenic
Disease IGG receptor I
Variation info
Gene HIST2H2BF FCGR1A
CLNDBN IGG receptor I, phagocytic, familial deficiency of
Reversed 0
HGVS NC_000001.10:g.149755780C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015950.26,