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rs748302886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748302886(C;T)
Make rs748302886(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2496827
GeneTBC1D24
is asnp
is mentioned by
dbSNPrs748302886
dbSNP (classic)rs748302886
ClinGenrs748302886
ebirs748302886
HLIrs748302886
Exacrs748302886
Gnomadrs748302886
Varsomers748302886
LitVarrs748302886
Maprs748302886
PheGenIrs748302886
Biobankrs748302886
1000 genomesrs748302886
hgdprs748302886
ensemblrs748302886
geneviewrs748302886
scholarrs748302886
googlers748302886
pharmgkbrs748302886
gwascentralrs748302886
openSNPrs748302886
23andMers748302886
SNPshotrs748302886
SNPdbers748302886
MSV3drs748302886
GWAS Ctlgrs748302886
Max Magnitude0
ClinVar
Risk rs748302886(T;T)
Alt rs748302886(T;T)
Reference Rs748302886(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBC1D24
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2546828C>T
CLNSRC
CLNACC RCV000492824.1,