rs397516208

Orientation

minus

Stabilized

minus

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

Make rs397516208(A;A)

Make rs397516208(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23417580

Gene	MHRT, MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs397516208
dbSNP (classic)	rs397516208
ClinGen	rs397516208
ebi	rs397516208
HLI	rs397516208
Exac	rs397516208
Gnomad	rs397516208
Varsome	rs397516208
LitVar	rs397516208
Map	rs397516208
PheGenI	rs397516208
Biobank	rs397516208
1000 genomes	rs397516208
hgdp	rs397516208
ensembl	rs397516208
geneview	rs397516208
scholar	rs397516208
google	rs397516208
pharmgkb	rs397516208
gwascentral	rs397516208
openSNP	rs397516208
23andMe	rs397516208
SNPshot	rs397516208
SNPdbe	rs397516208
MSV3d	rs397516208
GWAS Ctlg	rs397516208

Max Magnitude

0

ClinVar
Risk	rs397516208(A;A)
Alt	rs397516208(A;A)
Reference	Rs397516208(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	MYH7 MIR208B MHRT
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000014.8:g.23886789C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000035899.4, RCV000417392.1,