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rs202100019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202100019(C;T)
Make rs202100019(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position73850446
GeneLOC105374806, STAMBP
is asnp
is mentioned by
dbSNPrs202100019
dbSNP (old)rs202100019
ClinGenrs202100019
ebirs202100019
HLIrs202100019
Exacrs202100019
Gnomadrs202100019
Varsomers202100019
LitVarrs202100019
Maprs202100019
PheGenIrs202100019
Biobankrs202100019
1000 genomesrs202100019
hgdprs202100019
ensemblrs202100019
gopubmedrs202100019
geneviewrs202100019
scholarrs202100019
googlers202100019
pharmgkbrs202100019
gwascentralrs202100019
openSNPrs202100019
23andMers202100019
23andMe allrs202100019
SNPshotrs202100019
SNPdbers202100019
MSV3drs202100019
GWAS Ctlgrs202100019
Max Magnitude0
ClinVar
Risk rs202100019(T;T)
Alt rs202100019(T;T)
Reference Rs202100019(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene STAMBP
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.74077573C>T
CLNSRC
CLNACC RCV000487330.1,