rs397516979

Orientation

plus

Stabilized

plus

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

Make rs397516979(-;TCT)

Make rs397516979(TCT;TCT)

Reference

GRCh38 38.1/141

Chromosome

17

Position

39724744

Gene	ERBB2, MIR4728

is a	snp
is	mentioned by
dbSNP	rs397516979
dbSNP (classic)	rs397516979
ClinGen	rs397516979
ebi	rs397516979
HLI	rs397516979
Exac	rs397516979
Gnomad	rs397516979
Varsome	rs397516979
LitVar	rs397516979
Map	rs397516979
PheGenI	rs397516979
Biobank	rs397516979
1000 genomes	rs397516979
hgdp	rs397516979
ensembl	rs397516979
geneview	rs397516979
scholar	rs397516979
google	rs397516979
pharmgkb	rs397516979
gwascentral	rs397516979
openSNP	rs397516979
23andMe	rs397516979
SNPshot	rs397516979
SNPdbe	rs397516979
MSV3d	rs397516979
GWAS Ctlg	rs397516979

Max Magnitude

0

ClinVar
Risk	rs397516979(TCT;TCT) rs397516979(TGT;TGT) rs397516979(TTT;TTT)
Alt	rs397516979(TCT;TCT) rs397516979(TGT;TGT) rs397516979(TTT;TTT)
Reference	Rs397516979(-;-)
Significance	Probable-Pathogenic
Disease	not specified Non-small cell lung cancer Neoplasm of breast
Variation	info
Gene	MIR4728 ERBB2
CLNDBN	not specified Non-small cell lung cancer Neoplasm of breast
Reversed	0
HGVS	NC_000017.10:g.37880997_37880998insTCT; NC_000017.10:g.37880997_37880998insTGT; NC_000017.10:g.37880997_37880998insTTT
CLNSRC	ClinVar
CLNACC	RCV000038126.2, RCV000038127.3, RCV000431743.1, RCV000038128.2,