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rs1057520576

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520576(G;G)
Make rs1057520576(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position39243962
GenePDGFB
is asnp
is mentioned by
dbSNPrs1057520576
dbSNP (old)rs1057520576
ClinGenrs1057520576
ebirs1057520576
HLIrs1057520576
Exacrs1057520576
Gnomadrs1057520576
Varsomers1057520576
Maprs1057520576
PheGenIrs1057520576
Biobankrs1057520576
1000 genomesrs1057520576
hgdprs1057520576
ensemblrs1057520576
gopubmedrs1057520576
geneviewrs1057520576
scholarrs1057520576
googlers1057520576
pharmgkbrs1057520576
gwascentralrs1057520576
openSNPrs1057520576
23andMers1057520576
23andMe allrs1057520576
SNPshotrs1057520576
SNPdbers1057520576
MSV3drs1057520576
GWAS Ctlgrs1057520576
Max Magnitude0
ClinVar
Risk rs1057520576(G;G)
Alt rs1057520576(G;G)
Reference Rs1057520576(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PDGFB
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.39639967A>C
CLNSRC
CLNACC RCV000441852.1,