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rs1057524307

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524307(A;A)
Make rs1057524307(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position79921660
GeneELOVL4
is asnp
is mentioned by
dbSNPrs1057524307
dbSNP (old)rs1057524307
ClinGenrs1057524307
ebirs1057524307
HLIrs1057524307
Exacrs1057524307
Gnomadrs1057524307
Varsomers1057524307
LitVarrs1057524307
Maprs1057524307
PheGenIrs1057524307
Biobankrs1057524307
1000 genomesrs1057524307
hgdprs1057524307
ensemblrs1057524307
gopubmedrs1057524307
geneviewrs1057524307
scholarrs1057524307
googlers1057524307
pharmgkbrs1057524307
gwascentralrs1057524307
openSNPrs1057524307
23andMers1057524307
23andMe allrs1057524307
SNPshotrs1057524307
SNPdbers1057524307
MSV3drs1057524307
GWAS Ctlgrs1057524307
Max Magnitude0
ClinVar
Risk rs1057524307(A;A)
Alt rs1057524307(A;A)
Reference Rs1057524307(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELOVL4
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.80631377C>T
CLNSRC
CLNACC RCV000430736.1,