Have questions? Visit https://www.reddit.com/r/SNPedia

rs14251

From SNPedia

Orientationplus
Make rs14251(A;A)
Make rs14251(A;C)
Make rs14251(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position141639543
GeneFCHSD1, RELL2
is asnp
is mentioned by
dbSNPrs14251
ebirs14251
HLIrs14251
Exacrs14251
Varsomers14251
Maprs14251
PheGenIrs14251
hapmaprs14251
1000 genomesrs14251
hgdprs14251
ensemblrs14251
gopubmedrs14251
geneviewrs14251
scholarrs14251
googlers14251
pharmgkbrs14251
gwascentralrs14251
openSNPrs14251
23andMers14251
23andMe allrs14251
SNP Nexus

SNPshotrs14251
SNPdbers14251
MSV3drs14251
GWAS Ctlgrs14251
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 27573569] Two-stage additional evidence support association of common variants in the HDAC3 with the increasing risk of schizophrenia susceptibility.