rs397516978

Orientation

plus

Stabilized

plus

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

Make rs397516978(-;-)

Make rs397516978(-;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

39724738

Gene	ERBB2, MIR4728

is a	snp
is	mentioned by
dbSNP	rs397516978
dbSNP (classic)	rs397516978
ClinGen	rs397516978
ebi	rs397516978
HLI	rs397516978
Exac	rs397516978
Gnomad	rs397516978
Varsome	rs397516978
LitVar	rs397516978
Map	rs397516978
PheGenI	rs397516978
Biobank	rs397516978
1000 genomes	rs397516978
hgdp	rs397516978
ensembl	rs397516978
geneview	rs397516978
scholar	rs397516978
google	rs397516978
pharmgkb	rs397516978
gwascentral	rs397516978
openSNP	rs397516978
23andMe	rs397516978
SNPshot	rs397516978
SNPdbe	rs397516978
MSV3d	rs397516978
GWAS Ctlg	rs397516978

Max Magnitude

0

ClinVar
Risk	rs397516978(-;-)
Alt	rs397516978(-;-)
Reference	Rs397516978(A;A)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer
Variation	info
Gene	MIR4728 ERBB2
CLNDBN	Non-small cell lung cancer
Reversed	0
HGVS	NC_000017.10:g.37880991delA
CLNSRC	ClinVar
CLNACC	RCV000038125.2,