rs863223336

Orientation

plus

Stabilized

plus

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

Make rs863223336(-;-)

Make rs863223336(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63666067

Gene	RTEL1, RTEL1-TNFRSF6B

is a	snp
is	mentioned by
dbSNP	rs863223336
dbSNP (classic)	rs863223336
ClinGen	rs863223336
ebi	rs863223336
HLI	rs863223336
Exac	rs863223336
Gnomad	rs863223336
Varsome	rs863223336
LitVar	rs863223336
Map	rs863223336
PheGenI	rs863223336
Biobank	rs863223336
1000 genomes	rs863223336
hgdp	rs863223336
ensembl	rs863223336
geneview	rs863223336
scholar	rs863223336
google	rs863223336
pharmgkb	rs863223336
gwascentral	rs863223336
openSNP	rs863223336
23andMe	rs863223336
SNPshot	rs863223336
SNPdbe	rs863223336
MSV3d	rs863223336
GWAS Ctlg	rs863223336

Max Magnitude

0

ClinVar
Risk	rs863223336(-;-)
Alt	rs863223336(-;-)
Reference	Rs863223336(G;G)
Significance	Pathogenic
Disease	Pulmonary fibrosis and/or bone marrow failure
Variation	info
Gene	RTEL1-TNFRSF6B RTEL1
CLNDBN	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3
Reversed	0
HGVS	NC_000020.10:g.62297420delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170593.4,