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rs1057520507

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520507(C;T)
Make rs1057520507(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7224972
GeneACADVL, DVL2, MIR324
is asnp
is mentioned by
dbSNPrs1057520507
dbSNP (old)rs1057520507
ClinGenrs1057520507
ebirs1057520507
HLIrs1057520507
Exacrs1057520507
Gnomadrs1057520507
Varsomers1057520507
Maprs1057520507
PheGenIrs1057520507
Biobankrs1057520507
1000 genomesrs1057520507
hgdprs1057520507
ensemblrs1057520507
gopubmedrs1057520507
geneviewrs1057520507
scholarrs1057520507
googlers1057520507
pharmgkbrs1057520507
gwascentralrs1057520507
openSNPrs1057520507
23andMers1057520507
23andMe allrs1057520507
SNPshotrs1057520507
SNPdbers1057520507
MSV3drs1057520507
GWAS Ctlgrs1057520507
Max Magnitude0
ClinVar
Risk rs1057520507(T;T)
Alt rs1057520507(T;T)
Reference Rs1057520507(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324 DVL2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7128291C>T
CLNSRC
CLNACC RCV000438504.1,