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rs199422317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199422317(C;C)
Make rs199422317(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24240618
GeneTINF2
is asnp
is mentioned by
dbSNPrs199422317
ebirs199422317
HLIrs199422317
Exacrs199422317
Varsomers199422317
Maprs199422317
PheGenIrs199422317
hapmaprs199422317
1000 genomesrs199422317
hgdprs199422317
ensemblrs199422317
gopubmedrs199422317
geneviewrs199422317
scholarrs199422317
googlers199422317
pharmgkbrs199422317
gwascentralrs199422317
openSNPrs199422317
23andMers199422317
23andMe allrs199422317
SNP Nexus

SNPshotrs199422317
SNPdbers199422317
MSV3drs199422317
GWAS Ctlgrs199422317
Max Magnitude0
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,