rs397514742

Orientation

plus

Stabilized

plus

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

Make rs397514742(A;T)

Make rs397514742(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

3412301

Gene

PRDM16

is a	snp
is	mentioned by
dbSNP	rs397514742
dbSNP (classic)	rs397514742
ClinGen	rs397514742
ebi	rs397514742
HLI	rs397514742
Exac	rs397514742
Gnomad	rs397514742
Varsome	rs397514742
LitVar	rs397514742
Map	rs397514742
PheGenI	rs397514742
Biobank	rs397514742
1000 genomes	rs397514742
hgdp	rs397514742
ensembl	rs397514742
geneview	rs397514742
scholar	rs397514742
google	rs397514742
pharmgkb	rs397514742
gwascentral	rs397514742
openSNP	rs397514742
23andMe	rs397514742
SNPshot	rs397514742
SNPdbe	rs397514742
MSV3d	rs397514742
GWAS Ctlg	rs397514742

Max Magnitude

0

ClinVar
Risk	rs397514742(T;T)
Alt	rs397514742(T;T)
Reference	Rs397514742(A;A)
Significance	Pathogenic
Disease	Left ventricular noncompaction 8
Variation	info
Gene	PRDM16
CLNDBN	Left ventricular noncompaction 8
Reversed	0
HGVS	NC_000001.10:g.3328865A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000054518.3,