rs368282893

Orientation

plus

Stabilized

plus

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

Make rs368282893(C;T)

Make rs368282893(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

178782297

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs368282893
dbSNP (classic)	rs368282893
ClinGen	rs368282893
ebi	rs368282893
HLI	rs368282893
Exac	rs368282893
Gnomad	rs368282893
Varsome	rs368282893
LitVar	rs368282893
Map	rs368282893
PheGenI	rs368282893
Biobank	rs368282893
1000 genomes	rs368282893
hgdp	rs368282893
ensembl	rs368282893
geneview	rs368282893
scholar	rs368282893
google	rs368282893
pharmgkb	rs368282893
gwascentral	rs368282893
openSNP	rs368282893
23andMe	rs368282893
SNPshot	rs368282893
SNPdbe	rs368282893
MSV3d	rs368282893
GWAS Ctlg	rs368282893

Max Magnitude

0

ClinVar
Risk	rs368282893(T;T)
Alt	rs368282893(T;T)
Reference	Rs368282893(C;C)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	TTN
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000002.11:g.179647024C>T
CLNSRC
CLNACC	RCV000040208.2, RCV000171326.1,