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rs7591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs7591(A;T)
Make rs7591(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position65528964
GeneAXIN2
is asnp
is mentioned by
dbSNPrs7591
dbSNP (old)rs7591
ClinGenrs7591
ebirs7591
HLIrs7591
Exacrs7591
Gnomadrs7591
Varsomers7591
Maprs7591
PheGenIrs7591
Biobankrs7591
1000 genomesrs7591
hgdprs7591
ensemblrs7591
gopubmedrs7591
geneviewrs7591
scholarrs7591
googlers7591
pharmgkbrs7591
gwascentralrs7591
openSNPrs7591
23andMers7591
23andMe allrs7591
SNP Nexus

SNPshotrs7591
SNPdbers7591
MSV3drs7591
GWAS Ctlgrs7591
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 24484320] The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population


ClinVar
Risk rs7591(T;T)
Alt rs7591(T;T)
Reference Rs7591(A;A)
Significance Non-pathogenic
Disease Oligodontia-colorectal cancer syndrome
Variation info
Gene AXIN2
CLNDBN Oligodontia-colorectal cancer syndrome
Reversed 0
HGVS NC_000017.10:g.63525082A>T
CLNSRC
CLNACC RCV000333066.1,