rs397516199

Orientation

minus

Stabilized

minus

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

Make rs397516199(C;T)

Make rs397516199(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23418375

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs397516199
dbSNP (classic)	rs397516199
ClinGen	rs397516199
ebi	rs397516199
HLI	rs397516199
Exac	rs397516199
Gnomad	rs397516199
Varsome	rs397516199
LitVar	rs397516199
Map	rs397516199
PheGenI	rs397516199
Biobank	rs397516199
1000 genomes	rs397516199
hgdp	rs397516199
ensembl	rs397516199
geneview	rs397516199
scholar	rs397516199
google	rs397516199
pharmgkb	rs397516199
gwascentral	rs397516199
openSNP	rs397516199
23andMe	rs397516199
SNPshot	rs397516199
SNPdbe	rs397516199
MSV3d	rs397516199
GWAS Ctlg	rs397516199

Max Magnitude

0

ClinVar
Risk	rs397516199(T;T)
Alt	rs397516199(T;T)
Reference	Rs397516199(C;C)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	MYH7 MIR208B
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000014.8:g.23887584G>A
CLNSRC	ClinVar
CLNACC	RCV000035881.3, RCV000484605.1,