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rs770551610

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770551610(G;T)
Make rs770551610(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position50382603
GeneIKZF1, LOC105375275
is asnp
is mentioned by
dbSNPrs770551610
ebirs770551610
HLIrs770551610
Exacrs770551610
Varsomers770551610
Maprs770551610
PheGenIrs770551610
hapmaprs770551610
1000 genomesrs770551610
hgdprs770551610
ensemblrs770551610
gopubmedrs770551610
geneviewrs770551610
scholarrs770551610
googlers770551610
pharmgkbrs770551610
gwascentralrs770551610
openSNPrs770551610
23andMers770551610
23andMe allrs770551610
SNP Nexus

SNPshotrs770551610
SNPdbers770551610
MSV3drs770551610
GWAS Ctlgrs770551610
Max Magnitude0
ClinVar
Risk rs770551610(A,T;A,T)
Alt rs770551610(A,T;A,T)
Reference rs770551610(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IKZF1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.50450301G>A; NC_000007.13:g.50450301G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210346.2, RCV000210351.2,