rs587776805

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs587776805(-;TGTGGGCTC)

Make rs587776805(TGTGGGCTC;TGTGGGCTC)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

39724754

Gene	ERBB2, MIR4728

is a	snp
is	mentioned by
dbSNP	rs587776805
dbSNP (classic)	rs587776805
ClinGen	rs587776805
ebi	rs587776805
HLI	rs587776805
Exac	rs587776805
Gnomad	rs587776805
Varsome	rs587776805
LitVar	rs587776805
Map	rs587776805
PheGenI	rs587776805
Biobank	rs587776805
1000 genomes	rs587776805
hgdp	rs587776805
ensembl	rs587776805
geneview	rs587776805
scholar	rs587776805
google	rs587776805
pharmgkb	rs587776805
gwascentral	rs587776805
openSNP	rs587776805
23andMe	rs587776805
SNPshot	rs587776805
SNPdbe	rs587776805
MSV3d	rs587776805
GWAS Ctlg	rs587776805

Max Magnitude

0

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	RCV000014890.5,