Have questions? Visit https://www.reddit.com/r/SNPedia

rs10497203

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10497203(A;C)
Make rs10497203(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position158994911
GeneTANC1
is asnp
is mentioned by
dbSNPrs10497203
dbSNP (classic)rs10497203
ClinGenrs10497203
ebirs10497203
HLIrs10497203
Exacrs10497203
Gnomadrs10497203
Varsomers10497203
LitVarrs10497203
Maprs10497203
PheGenIrs10497203
Biobankrs10497203
1000 genomesrs10497203
hgdprs10497203
ensemblrs10497203
geneviewrs10497203
scholarrs10497203
googlers10497203
pharmgkbrs10497203
gwascentralrs10497203
openSNPrs10497203
23andMers10497203
SNPshotrs10497203
SNPdbers10497203
MSV3drs10497203
GWAS Ctlgrs10497203
Max Magnitude0
? (A;A) (A;C) (C;C) 28


ClinVar
Risk rs10497203(C;C)
Alt rs10497203(C;C)
Reference Rs10497203(A;A)
Significance Drug-response
Disease radiotherapy response - Toxicity/ADR
Variation info
Gene TANC1
CLNDBN radiotherapy response - Toxicity/ADR
Reversed 0
HGVS NC_000002.11:g.159851423A>C
CLNSRC PharmGKB Clinical Annotation
CLNACC RCV000211412.1,