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rs368207076

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs368207076(G;G)
Make rs368207076(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position128345551
GeneSLC27A4
is asnp
is mentioned by
dbSNPrs368207076
ebirs368207076
HLIrs368207076
Exacrs368207076
Varsomers368207076
Maprs368207076
PheGenIrs368207076
hapmaprs368207076
1000 genomesrs368207076
hgdprs368207076
ensemblrs368207076
gopubmedrs368207076
geneviewrs368207076
scholarrs368207076
googlers368207076
pharmgkbrs368207076
gwascentralrs368207076
openSNPrs368207076
23andMers368207076
23andMe allrs368207076
SNP Nexus

SNPshotrs368207076
SNPdbers368207076
MSV3drs368207076
GWAS Ctlgrs368207076
Max Magnitude0
ClinVar
Risk rs368207076(G;G)
Alt rs368207076(G;G)
Reference rs368207076(T;T)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SLC27A4
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000009.11:g.131107830T>G
CLNSRC
CLNACC RCV000210701.1,