rs786205702

Orientation

plus

Stabilized

plus

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

Make rs786205702(A;C)

Make rs786205702(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

20

Position

63695093

Gene	RTEL1, RTEL1-TNFRSF6B, TNFRSF6B

is a	snp
is	mentioned by
dbSNP	rs786205702
dbSNP (classic)	rs786205702
ClinGen	rs786205702
ebi	rs786205702
HLI	rs786205702
Exac	rs786205702
Gnomad	rs786205702
Varsome	rs786205702
LitVar	rs786205702
Map	rs786205702
PheGenI	rs786205702
Biobank	rs786205702
1000 genomes	rs786205702
hgdp	rs786205702
ensembl	rs786205702
geneview	rs786205702
scholar	rs786205702
google	rs786205702
pharmgkb	rs786205702
gwascentral	rs786205702
openSNP	rs786205702
23andMe	rs786205702
SNPshot	rs786205702
SNPdbe	rs786205702
MSV3d	rs786205702
GWAS Ctlg	rs786205702

Max Magnitude

0

ClinVar
Risk	rs786205702(C;C)
Alt	rs786205702(C;C)
Reference	Rs786205702(A;A)
Significance	Pathogenic
Disease	Pulmonary fibrosis and/or bone marrow failure
Variation	info
Gene	RTEL1-TNFRSF6B RTEL1 TNFRSF6B
CLNDBN	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3
Reversed	0
HGVS	NC_000020.10:g.62326446A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170596.3,