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rs2816216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2816216(C;C)
Make rs2816216(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position179206613
GeneABL2
is asnp
is mentioned by
dbSNPrs2816216
ebirs2816216
HLIrs2816216
Exacrs2816216
Varsomers2816216
Maprs2816216
PheGenIrs2816216
hapmaprs2816216
1000 genomesrs2816216
hgdprs2816216
ensemblrs2816216
gopubmedrs2816216
geneviewrs2816216
scholarrs2816216
googlers2816216
pharmgkbrs2816216
gwascentralrs2816216
openSNPrs2816216
23andMers2816216
23andMe allrs2816216
SNP Nexus

SNPshotrs2816216
SNPdbers2816216
MSV3drs2816216
GWAS Ctlgrs2816216
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM612005
DescCELIAC DISEASE, SUSCEPTIBILITY TO, 7; CELIAC7
Variant
Relatedalso