rs397516196

Orientation

minus

Stabilized

minus

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

Make rs397516196(A;A)

Make rs397516196(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23419293

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs397516196
dbSNP (classic)	rs397516196
ClinGen	rs397516196
ebi	rs397516196
HLI	rs397516196
Exac	rs397516196
Gnomad	rs397516196
Varsome	rs397516196
LitVar	rs397516196
Map	rs397516196
PheGenI	rs397516196
Biobank	rs397516196
1000 genomes	rs397516196
hgdp	rs397516196
ensembl	rs397516196
geneview	rs397516196
scholar	rs397516196
google	rs397516196
pharmgkb	rs397516196
gwascentral	rs397516196
openSNP	rs397516196
23andMe	rs397516196
SNPshot	rs397516196
SNPdbe	rs397516196
MSV3d	rs397516196
GWAS Ctlg	rs397516196

Max Magnitude

0

ClinVar
Risk	rs397516196(A;A)
Alt	rs397516196(A;A)
Reference	Rs397516196(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7 MIR208B
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23888502C>T
CLNSRC	ClinVar
CLNACC	RCV000035871.3,