rs606231469

Orientation

plus

Stabilized

plus

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

Make rs606231469(A;A)

Make rs606231469(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

74369495

Gene	FPGT-TNNI3K, TNNI3K

is a	snp
is	mentioned by
dbSNP	rs606231469
dbSNP (classic)	rs606231469
ClinGen	rs606231469
ebi	rs606231469
HLI	rs606231469
Exac	rs606231469
Gnomad	rs606231469
Varsome	rs606231469
LitVar	rs606231469
Map	rs606231469
PheGenI	rs606231469
Biobank	rs606231469
1000 genomes	rs606231469
hgdp	rs606231469
ensembl	rs606231469
geneview	rs606231469
scholar	rs606231469
google	rs606231469
pharmgkb	rs606231469
gwascentral	rs606231469
openSNP	rs606231469
23andMe	rs606231469
SNPshot	rs606231469
SNPdbe	rs606231469
MSV3d	rs606231469
GWAS Ctlg	rs606231469

Max Magnitude

0

ClinVar
Risk	rs606231469(A;A)
Alt	rs606231469(A;A)
Reference	Rs606231469(G;G)
Significance	Pathogenic
Disease	Cardiac conduction disease with or without dilated cardiomyopathy
Variation	info
Gene	TNNI3K FPGT-TNNI3K
CLNDBN	Cardiac conduction disease with or without dilated cardiomyopathy
Reversed	0
HGVS	NC_000001.10:g.74835179G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000148950.4,