rs199422317

Orientation

minus

Stabilized

minus

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

Make rs199422317(C;C)

Make rs199422317(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

24240618

Gene

TINF2

is a	snp
is	mentioned by
dbSNP	rs199422317
dbSNP (classic)	rs199422317
ClinGen	rs199422317
ebi	rs199422317
HLI	rs199422317
Exac	rs199422317
Gnomad	rs199422317
Varsome	rs199422317
LitVar	rs199422317
Map	rs199422317
PheGenI	rs199422317
Biobank	rs199422317
1000 genomes	rs199422317
hgdp	rs199422317
ensembl	rs199422317
geneview	rs199422317
scholar	rs199422317
google	rs199422317
pharmgkb	rs199422317
gwascentral	rs199422317
openSNP	rs199422317
23andMe	rs199422317
SNPshot	rs199422317
SNPdbe	rs199422317
MSV3d	rs199422317
GWAS Ctlg	rs199422317

Max Magnitude

0

ClinVar
Risk	rs199422317(C;C)
Alt	rs199422317(C;C)
Reference	Rs199422317(T;T)
Significance	Pathogenic
Disease	Aplastic anemia
Variation	info
Gene	TINF2
CLNDBN	Aplastic anemia
Reversed	1
HGVS	NC_000014.8:g.24709824A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032176.1,