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rs869312967

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312967(A;A)
Make rs869312967(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position128355796
GeneSLC27A4
is asnp
is mentioned by
dbSNPrs869312967
ebirs869312967
HLIrs869312967
Exacrs869312967
Varsomers869312967
Maprs869312967
PheGenIrs869312967
hapmaprs869312967
1000 genomesrs869312967
hgdprs869312967
ensemblrs869312967
gopubmedrs869312967
geneviewrs869312967
scholarrs869312967
googlers869312967
pharmgkbrs869312967
gwascentralrs869312967
openSNPrs869312967
23andMers869312967
23andMe allrs869312967
SNP Nexus

SNPshotrs869312967
SNPdbers869312967
MSV3drs869312967
GWAS Ctlgrs869312967
Max Magnitude0
ClinVar
Risk rs869312967(A;A)
Alt rs869312967(A;A)
Reference rs869312967(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SLC27A4
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000009.11:g.131118075G>A
CLNSRC
CLNACC RCV000210621.1,