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rs1057518098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518098(-;TAAT)
Make rs1057518098(TAAT;TAAT)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position86643827
GeneCNGB3
is asnp
is mentioned by
dbSNPrs1057518098
dbSNP (old)rs1057518098
ClinGenrs1057518098
ebirs1057518098
HLIrs1057518098
Exacrs1057518098
Gnomadrs1057518098
Varsomers1057518098
LitVarrs1057518098
Maprs1057518098
PheGenIrs1057518098
Biobankrs1057518098
1000 genomesrs1057518098
hgdprs1057518098
ensemblrs1057518098
gopubmedrs1057518098
geneviewrs1057518098
scholarrs1057518098
googlers1057518098
pharmgkbrs1057518098
gwascentralrs1057518098
openSNPrs1057518098
23andMers1057518098
23andMe allrs1057518098
SNPshotrs1057518098
SNPdbers1057518098
MSV3drs1057518098
GWAS Ctlgrs1057518098
Max Magnitude0
ClinVar
Risk rs1057518098(TAAT;TAAT)
Alt rs1057518098(TAAT;TAAT)
Reference Rs1057518098(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGB3
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.87656056_87656059dupATTA
CLNSRC
CLNACC RCV000412821.1,