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rs139805921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139805921(A;A)
Make rs139805921(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position42388935
GeneTMPRSS3
is asnp
is mentioned by
dbSNPrs139805921
dbSNP (old)rs139805921
ClinGenrs139805921
ebirs139805921
HLIrs139805921
Exacrs139805921
Gnomadrs139805921
Varsomers139805921
LitVarrs139805921
Maprs139805921
PheGenIrs139805921
Biobankrs139805921
1000 genomesrs139805921
hgdprs139805921
ensemblrs139805921
gopubmedrs139805921
geneviewrs139805921
scholarrs139805921
googlers139805921
pharmgkbrs139805921
gwascentralrs139805921
openSNPrs139805921
23andMers139805921
23andMe allrs139805921
SNPshotrs139805921
SNPdbers139805921
MSV3drs139805921
GWAS Ctlgrs139805921
Max Magnitude0
ClinVar
Risk rs139805921(A;A)
Alt rs139805921(A;A)
Reference Rs139805921(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMPRSS3
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.43809044G>A
CLNSRC
CLNACC RCV000441150.1,