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rs796051982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796051982(-;GTG)
Make rs796051982(GTG;GTG)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40411272
GeneIVD
is asnp
is mentioned by
dbSNPrs796051982
ClinGenrs796051982
ebirs796051982
HLIrs796051982
Exacrs796051982
Varsomers796051982
Maprs796051982
PheGenIrs796051982
hapmaprs796051982
1000 genomesrs796051982
hgdprs796051982
ensemblrs796051982
gopubmedrs796051982
geneviewrs796051982
scholarrs796051982
googlers796051982
pharmgkbrs796051982
gwascentralrs796051982
openSNPrs796051982
23andMers796051982
23andMe allrs796051982
SNP Nexus

SNPshotrs796051982
SNPdbers796051982
MSV3drs796051982
GWAS Ctlgrs796051982
Max Magnitude0
ClinVar
Risk rs796051982(GTG;GTG)
Alt rs796051982(GTG;GTG)
Reference Rs796051982(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40703469_40703471dupGTG
CLNSRC
CLNACC RCV000185985.1,