rs776744306

Orientation

plus

Stabilized

plus

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

Make rs776744306(C;C)

Make rs776744306(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63690442

Gene	RTEL1, RTEL1-TNFRSF6B

is a	snp
is	mentioned by
dbSNP	rs776744306
dbSNP (classic)	rs776744306
ClinGen	rs776744306
ebi	rs776744306
HLI	rs776744306
Exac	rs776744306
Gnomad	rs776744306
Varsome	rs776744306
LitVar	rs776744306
Map	rs776744306
PheGenI	rs776744306
Biobank	rs776744306
1000 genomes	rs776744306
hgdp	rs776744306
ensembl	rs776744306
geneview	rs776744306
scholar	rs776744306
google	rs776744306
pharmgkb	rs776744306
gwascentral	rs776744306
openSNP	rs776744306
23andMe	rs776744306
SNPshot	rs776744306
SNPdbe	rs776744306
MSV3d	rs776744306
GWAS Ctlg	rs776744306

Max Magnitude

0

ClinVar
Risk	rs776744306(A;A) rs776744306(C;C)
Alt	rs776744306(A;A) rs776744306(C;C)
Reference	Rs776744306(G;G)
Significance	Pathogenic
Disease	Pulmonary fibrosis and/or bone marrow failure Idiopathic fibrosing alveolitis
Variation	info
Gene	RTEL1-TNFRSF6B RTEL1
CLNDBN	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3 Idiopathic fibrosing alveolitis, chronic form
Reversed	0
HGVS	NC_000020.10:g.62321795G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000201225.3, RCV000201651.1,