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rs174576

From SNPedia

Orientationplus
Stabilizedplus
Make rs174576(A;A)
Make rs174576(A;C)
Make rs174576(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position61836038
GeneFADS2
is asnp
is mentioned by
dbSNPrs174576
dbSNP (classic)rs174576
ClinGenrs174576
ebirs174576
HLIrs174576
Exacrs174576
Gnomadrs174576
Varsomers174576
LitVarrs174576
Maprs174576
PheGenIrs174576
Biobankrs174576
1000 genomesrs174576
hgdprs174576
ensemblrs174576
geneviewrs174576
scholarrs174576
googlers174576
pharmgkbrs174576
gwascentralrs174576
openSNPrs174576
23andMers174576
23andMe allrs174576
SNPshotrs174576
SNPdbers174576
MSV3drs174576
GWAS Ctlgrs174576
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 24819575] Common genetic variants and risk of brain injury after preterm birth


[PMID 30531795] Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population.