rs397516976

Orientation

plus

Stabilized

plus

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

Make rs397516976(-;ATACGTGATGGC)

Make rs397516976(ATACGTGATGGC;ATACGTGATGGC)

Reference

GRCh38 38.1/141

Chromosome

17

Position

39724742

Gene	ERBB2, MIR4728

is a	snp
is	mentioned by
dbSNP	rs397516976
dbSNP (classic)	rs397516976
ClinGen	rs397516976
ebi	rs397516976
HLI	rs397516976
Exac	rs397516976
Gnomad	rs397516976
Varsome	rs397516976
LitVar	rs397516976
Map	rs397516976
PheGenI	rs397516976
Biobank	rs397516976
1000 genomes	rs397516976
hgdp	rs397516976
ensembl	rs397516976
geneview	rs397516976
scholar	rs397516976
google	rs397516976
pharmgkb	rs397516976
gwascentral	rs397516976
openSNP	rs397516976
23andMe	rs397516976
SNPshot	rs397516976
SNPdbe	rs397516976
MSV3d	rs397516976
GWAS Ctlg	rs397516976

Max Magnitude

0

ClinVar
Risk	rs397516976(ATACGTGATGGC;ATACGTGATGGC) rs397516976(CTCCGTGATGGC;CTCCGTGATGGC)
Alt	rs397516976(ATACGTGATGGC;ATACGTGATGGC) rs397516976(CTCCGTGATGGC;CTCCGTGATGGC)
Reference	Rs397516976(-;-)
Significance	Pathogenic
Disease	Adenocarcinoma of lung Non-small cell lung cancer
Variation	info
Gene	MIR4728 ERBB2
CLNDBN	Adenocarcinoma of lung Non-small cell lung cancer
Reversed	0
HGVS	NC_000017.10:g.37880984_37880995dupATACGTGATGGC; NC_000017.10:g.37880995_37880996insCTCCGTGATGGC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014889.5, RCV000038123.2, RCV000156384.1,