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rs749890642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs749890642(A;A)
Make rs749890642(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position32089277
GeneTNXB
is asnp
is mentioned by
dbSNPrs749890642
dbSNP (classic)rs749890642
ClinGenrs749890642
ebirs749890642
HLIrs749890642
Exacrs749890642
Gnomadrs749890642
Varsomers749890642
LitVarrs749890642
Maprs749890642
PheGenIrs749890642
Biobankrs749890642
1000 genomesrs749890642
hgdprs749890642
ensemblrs749890642
geneviewrs749890642
scholarrs749890642
googlers749890642
pharmgkbrs749890642
gwascentralrs749890642
openSNPrs749890642
23andMers749890642
23andMe allrs749890642
SNPshotrs749890642
SNPdbers749890642
MSV3drs749890642
GWAS Ctlgrs749890642
Max Magnitude0
ClinVar
Risk rs749890642(A;A)
Alt rs749890642(A;A)
Reference Rs749890642(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNXB
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.32057054G>A
CLNSRC
CLNACC RCV000413590.1,