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rs1057521784

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521784(A;A)
Make rs1057521784(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position100105985
GeneAP4M1
is asnp
is mentioned by
dbSNPrs1057521784
dbSNP (old)rs1057521784
ClinGenrs1057521784
ebirs1057521784
HLIrs1057521784
Exacrs1057521784
Gnomadrs1057521784
Varsomers1057521784
Maprs1057521784
PheGenIrs1057521784
Biobankrs1057521784
1000 genomesrs1057521784
hgdprs1057521784
ensemblrs1057521784
gopubmedrs1057521784
geneviewrs1057521784
scholarrs1057521784
googlers1057521784
pharmgkbrs1057521784
gwascentralrs1057521784
openSNPrs1057521784
23andMers1057521784
23andMe allrs1057521784
SNPshotrs1057521784
SNPdbers1057521784
MSV3drs1057521784
GWAS Ctlgrs1057521784
Max Magnitude0
ClinVar
Risk rs1057521784(A;A)
Alt rs1057521784(A;A)
Reference Rs1057521784(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AP4M1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.99703608G>A
CLNSRC
CLNACC RCV000422720.1,