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rs72338773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in complete genomics
Make rs72338773(-;GGGCGCTGT)
Make rs72338773(GGGCGCTGT;GGGCGCTGT)
ReferenceGRCh37.p10 37.5/138
Chromosome17
Position46608203
GeneHOXB1
is asnp
is mentioned by
dbSNPrs72338773
ebirs72338773
HLIrs72338773
Exacrs72338773
Varsomers72338773
Maprs72338773
PheGenIrs72338773
hapmaprs72338773
1000 genomesrs72338773
hgdprs72338773
ensemblrs72338773
gopubmedrs72338773
geneviewrs72338773
scholarrs72338773
googlers72338773
pharmgkbrs72338773
gwascentralrs72338773
openSNPrs72338773
23andMers72338773
23andMe allrs72338773
SNP Nexus

SNPshotrs72338773
SNPdbers72338773
MSV3drs72338773
GWAS Ctlgrs72338773
StatusDeleted
Max Magnitude0

[PMID 20678259OA-icon.png] Candidate gene study of HOXB1 in autism spectrum disorder

[PMID 21980499OA-icon.png] An Integrated Meta-Analysis of Two Variants in HOXA1/HOXB1 and Their Effect on the Risk of Autism Spectrum Disorders