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rs756181906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756181906(G;T)
Make rs756181906(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2496828
GeneTBC1D24
is asnp
is mentioned by
dbSNPrs756181906
dbSNP (classic)rs756181906
ClinGenrs756181906
ebirs756181906
HLIrs756181906
Exacrs756181906
Gnomadrs756181906
Varsomers756181906
LitVarrs756181906
Maprs756181906
PheGenIrs756181906
Biobankrs756181906
1000 genomesrs756181906
hgdprs756181906
ensemblrs756181906
geneviewrs756181906
scholarrs756181906
googlers756181906
pharmgkbrs756181906
gwascentralrs756181906
openSNPrs756181906
23andMers756181906
SNPshotrs756181906
SNPdbers756181906
MSV3drs756181906
GWAS Ctlgrs756181906
Max Magnitude0
ClinVar
Risk rs756181906(A;A) rs756181906(T;T)
Alt rs756181906(A;A) rs756181906(T;T)
Reference Rs756181906(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBC1D24
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2546829G>T
CLNSRC
CLNACC RCV000189690.2,