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rs1057520088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520088(A;G)
Make rs1057520088(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7220945
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs1057520088
dbSNP (old)rs1057520088
ClinGenrs1057520088
ebirs1057520088
HLIrs1057520088
Exacrs1057520088
Gnomadrs1057520088
Varsomers1057520088
Maprs1057520088
PheGenIrs1057520088
Biobankrs1057520088
1000 genomesrs1057520088
hgdprs1057520088
ensemblrs1057520088
gopubmedrs1057520088
geneviewrs1057520088
scholarrs1057520088
googlers1057520088
pharmgkbrs1057520088
gwascentralrs1057520088
openSNPrs1057520088
23andMers1057520088
23andMe allrs1057520088
SNPshotrs1057520088
SNPdbers1057520088
MSV3drs1057520088
GWAS Ctlgrs1057520088
Max Magnitude0
ClinVar
Risk rs1057520088(G;G)
Alt rs1057520088(G;G)
Reference Rs1057520088(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124264A>G
CLNSRC
CLNACC RCV000432463.1,