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rs770551610

From SNPedia

Orientationplus
Stabilizedplus
Make rs770551610(G;T)
Make rs770551610(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position50382603
GeneIKZF1
is asnp
is mentioned by
dbSNPrs770551610
dbSNP (classic)rs770551610
ClinGenrs770551610
ebirs770551610
HLIrs770551610
Exacrs770551610
Gnomadrs770551610
Varsomers770551610
LitVarrs770551610
Maprs770551610
PheGenIrs770551610
Biobankrs770551610
1000 genomesrs770551610
hgdprs770551610
ensemblrs770551610
geneviewrs770551610
scholarrs770551610
googlers770551610
pharmgkbrs770551610
gwascentralrs770551610
openSNPrs770551610
23andMers770551610
SNPshotrs770551610
SNPdbers770551610
MSV3drs770551610
GWAS Ctlgrs770551610
Max Magnitude0
ClinVar
Risk rs770551610(A;A) rs770551610(T;T)
Alt rs770551610(A;A) rs770551610(T;T)
Reference Rs770551610(G;G)
Significance Pathogenic
Disease Immunodeficiency
Variation info
Gene IKZF1
CLNDBN Immunodeficiency, common variable, 13
Reversed 0
HGVS NC_000007.13:g.50450301G>A; NC_000007.13:g.50450301G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210346.2, RCV000210351.2,