rs774966208

Orientation

plus

Stabilized

plus

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

Make rs774966208(C;G)

Make rs774966208(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

136523014

Gene

NOTCH1

is a	snp
is	mentioned by
dbSNP	rs774966208
dbSNP (classic)	rs774966208
ClinGen	rs774966208
ebi	rs774966208
HLI	rs774966208
Exac	rs774966208
Gnomad	rs774966208
Varsome	rs774966208
LitVar	rs774966208
Map	rs774966208
PheGenI	rs774966208
Biobank	rs774966208
1000 genomes	rs774966208
hgdp	rs774966208
ensembl	rs774966208
geneview	rs774966208
scholar	rs774966208
google	rs774966208
pharmgkb	rs774966208
gwascentral	rs774966208
openSNP	rs774966208
23andMe	rs774966208
SNPshot	rs774966208
SNPdbe	rs774966208
MSV3d	rs774966208
GWAS Ctlg	rs774966208

Max Magnitude

0

ClinVar
Risk	rs774966208(G;G) rs774966208(T;T)
Alt	rs774966208(G;G) rs774966208(T;T)
Reference	Rs774966208(C;C)
Significance	Pathogenic
Disease	Tetralogy of Fallot
Variation	info
Gene	NOTCH1
CLNDBN	Tetralogy of Fallot
Reversed	0
HGVS	NC_000009.11:g.139417466C>T
CLNSRC
CLNACC	RCV000408653.1,