Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519169(A;A)
Make rs1057519169(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56096847
GeneERBB3
is asnp
is mentioned by
dbSNPrs1057519169
dbSNP (old)rs1057519169
ClinGenrs1057519169
ebirs1057519169
HLIrs1057519169
Exacrs1057519169
Gnomadrs1057519169
Varsomers1057519169
LitVarrs1057519169
Maprs1057519169
PheGenIrs1057519169
Biobankrs1057519169
1000 genomesrs1057519169
hgdprs1057519169
ensemblrs1057519169
gopubmedrs1057519169
geneviewrs1057519169
scholarrs1057519169
googlers1057519169
pharmgkbrs1057519169
gwascentralrs1057519169
openSNPrs1057519169
23andMers1057519169
23andMe allrs1057519169
SNPshotrs1057519169
SNPdbers1057519169
MSV3drs1057519169
GWAS Ctlgrs1057519169
Max Magnitude0
ClinVar
Risk rs1057519169(A;A)
Alt rs1057519169(A;A)
Reference Rs1057519169(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERBB3
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.56490631G>A
CLNSRC
CLNACC RCV000415949.1,