rs201850378

Orientation

plus

Stabilized

plus

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

Make rs201850378(C;T)

Make rs201850378(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

21815724

Gene

MIB1

is a	snp
is	mentioned by
dbSNP	rs201850378
dbSNP (classic)	rs201850378
ClinGen	rs201850378
ebi	rs201850378
HLI	rs201850378
Exac	rs201850378
Gnomad	rs201850378
Varsome	rs201850378
LitVar	rs201850378
Map	rs201850378
PheGenI	rs201850378
Biobank	rs201850378
1000 genomes	rs201850378
hgdp	rs201850378
ensembl	rs201850378
geneview	rs201850378
scholar	rs201850378
google	rs201850378
pharmgkb	rs201850378
gwascentral	rs201850378
openSNP	rs201850378
23andMe	rs201850378
SNPshot	rs201850378
SNPdbe	rs201850378
MSV3d	rs201850378
GWAS Ctlg	rs201850378

Max Magnitude

0

ClinVar
Risk	rs201850378(T;T)
Alt	rs201850378(T;T)
Reference	Rs201850378(C;C)
Significance	Pathogenic
Disease	Left ventricular noncompaction 7 not specified
Variation	info
Gene	MIB1
CLNDBN	Left ventricular noncompaction 7 not specified
Reversed	0
HGVS	NC_000018.9:g.19395685C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033170.2, RCV000485600.1,