rs863223792

Orientation

plus

Stabilized

plus

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

Make rs863223792(C;T)

Make rs863223792(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

218436110

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs863223792
dbSNP (classic)	rs863223792
ClinGen	rs863223792
ebi	rs863223792
HLI	rs863223792
Exac	rs863223792
Gnomad	rs863223792
Varsome	rs863223792
LitVar	rs863223792
Map	rs863223792
PheGenI	rs863223792
Biobank	rs863223792
1000 genomes	rs863223792
hgdp	rs863223792
ensembl	rs863223792
geneview	rs863223792
scholar	rs863223792
google	rs863223792
pharmgkb	rs863223792
gwascentral	rs863223792
openSNP	rs863223792
23andMe	rs863223792
SNPshot	rs863223792
SNPdbe	rs863223792
MSV3d	rs863223792
GWAS Ctlg	rs863223792

Max Magnitude

0

ClinVar
Risk	rs863223792(T;T)
Alt	rs863223792(T;T)
Reference	Rs863223792(C;C)
Significance	Other
Disease	not provided Loeys-Dietz syndrome 4
Variation	info
Gene	TGFB2
CLNDBN	not provided Loeys-Dietz syndrome 4
Reversed	0
HGVS	NC_000001.10:g.218609452C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000195710.3, RCV000210465.2,