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rs775739391

From SNPedia

Orientationplus
Make rs775739391(-;-)
Make rs775739391(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position33246807
GeneIFNAR2
is asnp
is mentioned by
dbSNPrs775739391
ebirs775739391
HLIrs775739391
Exacrs775739391
Varsomers775739391
Maprs775739391
PheGenIrs775739391
hapmaprs775739391
1000 genomesrs775739391
hgdprs775739391
ensemblrs775739391
gopubmedrs775739391
geneviewrs775739391
scholarrs775739391
googlers775739391
pharmgkbrs775739391
gwascentralrs775739391
openSNPrs775739391
23andMers775739391
23andMe allrs775739391
SNP Nexus

SNPshotrs775739391
SNPdbers775739391
MSV3drs775739391
GWAS Ctlgrs775739391
Max Magnitude
ClinVar
Risk rs775739391(;)
Alt rs775739391(;)
Reference rs775739391(A;A)
Significance Pathogenic
Disease Immunodeficiency 45
Variation info
Gene IFNAR2
CLNDBN Immunodeficiency 45
Reversed 0
HGVS NC_000021.8:g.34619112delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000202387.1,