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rs139484231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139484231(C;T)
Make rs139484231(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position42388523
GeneTMPRSS3
is asnp
is mentioned by
dbSNPrs139484231
dbSNP (classic)rs139484231
ClinGenrs139484231
ebirs139484231
HLIrs139484231
Exacrs139484231
Gnomadrs139484231
Varsomers139484231
LitVarrs139484231
Maprs139484231
PheGenIrs139484231
Biobankrs139484231
1000 genomesrs139484231
hgdprs139484231
ensemblrs139484231
geneviewrs139484231
scholarrs139484231
googlers139484231
pharmgkbrs139484231
gwascentralrs139484231
openSNPrs139484231
23andMers139484231
SNPshotrs139484231
SNPdbers139484231
MSV3drs139484231
GWAS Ctlgrs139484231
Max Magnitude0
ClinVar
Risk rs139484231(T;T)
Alt rs139484231(T;T)
Reference Rs139484231(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TMPRSS3
CLNDBN not specified not provided
Reversed 0
HGVS NC_000021.8:g.43808632C>T
CLNSRC
CLNACC RCV000178994.1, RCV000493533.1,