Have questions? Visit https://www.reddit.com/r/SNPedia

rs748026507

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs748026507(C;C)
Make rs748026507(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40407992
GeneIVD
is asnp
is mentioned by
dbSNPrs748026507
ebirs748026507
HLIrs748026507
Exacrs748026507
Varsomers748026507
Maprs748026507
PheGenIrs748026507
hapmaprs748026507
1000 genomesrs748026507
hgdprs748026507
ensemblrs748026507
gopubmedrs748026507
geneviewrs748026507
scholarrs748026507
googlers748026507
pharmgkbrs748026507
gwascentralrs748026507
openSNPrs748026507
23andMers748026507
23andMe allrs748026507
SNP Nexus

SNPshotrs748026507
SNPdbers748026507
MSV3drs748026507
GWAS Ctlgrs748026507
Max Magnitude0
ClinVar
Risk rs748026507(C;C)
Alt rs748026507(C;C)
Reference rs748026507(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40700191T>C
CLNSRC
CLNACC RCV000185982.1,