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rs1057520108

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520108(-;-)
Make rs1057520108(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39687983
GeneERBB2, PGAP3
is asnp
is mentioned by
dbSNPrs1057520108
dbSNP (old)rs1057520108
ClinGenrs1057520108
ebirs1057520108
HLIrs1057520108
Exacrs1057520108
Gnomadrs1057520108
Varsomers1057520108
Maprs1057520108
PheGenIrs1057520108
Biobankrs1057520108
1000 genomesrs1057520108
hgdprs1057520108
ensemblrs1057520108
gopubmedrs1057520108
geneviewrs1057520108
scholarrs1057520108
googlers1057520108
pharmgkbrs1057520108
gwascentralrs1057520108
openSNPrs1057520108
23andMers1057520108
23andMe allrs1057520108
SNPshotrs1057520108
SNPdbers1057520108
MSV3drs1057520108
GWAS Ctlgrs1057520108
Max Magnitude0
ClinVar
Risk rs1057520108(-;-)
Alt rs1057520108(-;-)
Reference Rs1057520108(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERBB2 PGAP3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.37844236delA
CLNSRC
CLNACC RCV000432634.1,