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rs765028734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs765028734(-;G)
Make rs765028734(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position32081646
GeneTNXB
is asnp
is mentioned by
dbSNPrs765028734
dbSNP (classic)rs765028734
ClinGenrs765028734
ebirs765028734
HLIrs765028734
Exacrs765028734
Gnomadrs765028734
Varsomers765028734
LitVarrs765028734
Maprs765028734
PheGenIrs765028734
Biobankrs765028734
1000 genomesrs765028734
hgdprs765028734
ensemblrs765028734
geneviewrs765028734
scholarrs765028734
googlers765028734
pharmgkbrs765028734
gwascentralrs765028734
openSNPrs765028734
23andMers765028734
23andMe allrs765028734
SNPshotrs765028734
SNPdbers765028734
MSV3drs765028734
GWAS Ctlgrs765028734
Max Magnitude0
ClinVar
Risk rs765028734(G;G) rs765028734(GG;GG)
Alt rs765028734(G;G) rs765028734(GG;GG)
Reference Rs765028734(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNXB
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.32049423_32049424insGG
CLNSRC
CLNACC RCV000487708.1,