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rs587776805

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776805(-;-)
Make rs587776805(-;TGTGGGCTC)
Make rs587776805(TGTGGGCTC;TGTGGGCTC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position39724754
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs587776805
ebirs587776805
HLIrs587776805
Exacrs587776805
Varsomers587776805
Maprs587776805
PheGenIrs587776805
hapmaprs587776805
1000 genomesrs587776805
hgdprs587776805
ensemblrs587776805
gopubmedrs587776805
geneviewrs587776805
scholarrs587776805
googlers587776805
pharmgkbrs587776805
gwascentralrs587776805
openSNPrs587776805
23andMers587776805
23andMe allrs587776805
SNP Nexus

SNPshotrs587776805
SNPdbers587776805
MSV3drs587776805
GWAS Ctlgrs587776805
Max Magnitude0
ClinVar
Risk rs587776805(TGTGGGCTC;TGTGGGCTC)
Alt rs587776805(TGTGGGCTC;TGTGGGCTC)
Reference rs587776805(;)
Significance Pathogenic
Disease Adenocarcinoma of lung
Variation info
Gene ERBB2 MIR4728
CLNDBN Adenocarcinoma of lung
Reversed 0
HGVS NC_000017.10:g.37880999_37881007dupTGTGGGCTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014890.4,