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rs479632

From SNPedia

Orientationminus
Stabilizedminus
Make rs479632(C;C)
Make rs479632(C;G)
Make rs479632(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position135028828
GenePITX1
is asnp
is mentioned by
dbSNPrs479632
ebirs479632
HLIrs479632
Exacrs479632
Varsomers479632
Maprs479632
PheGenIrs479632
hapmaprs479632
1000 genomesrs479632
hgdprs479632
ensemblrs479632
gopubmedrs479632
geneviewrs479632
scholarrs479632
googlers479632
pharmgkbrs479632
gwascentralrs479632
openSNPrs479632
23andMers479632
23andMe allrs479632
SNP Nexus

SNPshotrs479632
SNPdbers479632
MSV3drs479632
GWAS Ctlgrs479632
GMAF0.3182
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 20054692] Genetic polymorphism of PITX1 in susceptibility to knee osteoarthritis in a Chinese Han population: a case-control study


[PMID 18053270OA-icon.png] Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.


GET Evidence
PITX1-G299A
aa_change Gly299Ala
aa_change_short G299A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.215561
summary