rs398122883

Orientation

plus

Stabilized

plus

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

Make rs398122883(-;-)

Make rs398122883(-;CTACGCCAAGGAGGT)

Reference

GRCh38 38.1/141

Chromosome

1

Position

218346995

Gene	TGFB2, TGFB2-AS1

is a	snp
is	mentioned by
dbSNP	rs398122883
dbSNP (classic)	rs398122883
ClinGen	rs398122883
ebi	rs398122883
HLI	rs398122883
Exac	rs398122883
Gnomad	rs398122883
Varsome	rs398122883
LitVar	rs398122883
Map	rs398122883
PheGenI	rs398122883
Biobank	rs398122883
1000 genomes	rs398122883
hgdp	rs398122883
ensembl	rs398122883
geneview	rs398122883
scholar	rs398122883
google	rs398122883
pharmgkb	rs398122883
gwascentral	rs398122883
openSNP	rs398122883
23andMe	rs398122883
SNPshot	rs398122883
SNPdbe	rs398122883
MSV3d	rs398122883
GWAS Ctlg	rs398122883

Max Magnitude

0

ClinVar
Risk	rs398122883(-;-)
Alt	rs398122883(-;-)
Reference	Rs398122883(CTACGCCAAGGAGGT;CTACGCCAAGGAGGT)
Significance	Pathogenic
Disease	Loeys-Dietz syndrome 4 Holt-Oram syndrome
Variation	info
Gene	TGFB2 TGFB2-AS1
CLNDBN	Loeys-Dietz syndrome 4 Holt-Oram syndrome
Reversed	0
HGVS	NC_000001.10:g.218520337_218520351delCTACGCCAAGGAGGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030733.26, RCV000468724.1,