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rs199801224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199801224(C;T)
Make rs199801224(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position20043392
GeneTANGO2
is asnp
is mentioned by
dbSNPrs199801224
dbSNP (old)rs199801224
ClinGenrs199801224
ebirs199801224
HLIrs199801224
Exacrs199801224
Gnomadrs199801224
Varsomers199801224
LitVarrs199801224
Maprs199801224
PheGenIrs199801224
Biobankrs199801224
1000 genomesrs199801224
hgdprs199801224
ensemblrs199801224
gopubmedrs199801224
geneviewrs199801224
scholarrs199801224
googlers199801224
pharmgkbrs199801224
gwascentralrs199801224
openSNPrs199801224
23andMers199801224
23andMe allrs199801224
SNPshotrs199801224
SNPdbers199801224
MSV3drs199801224
GWAS Ctlgrs199801224
Max Magnitude0
ClinVar
Risk rs199801224(A;A) rs199801224(T;T)
Alt rs199801224(A;A) rs199801224(T;T)
Reference Rs199801224(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TANGO2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.20030915C>T
CLNSRC
CLNACC RCV000435649.1,