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rs747273828

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747273828(C;C)
Make rs747273828(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40407696
GeneIVD
is asnp
is mentioned by
dbSNPrs747273828
ebirs747273828
HLIrs747273828
Exacrs747273828
Varsomers747273828
Maprs747273828
PheGenIrs747273828
hapmaprs747273828
1000 genomesrs747273828
hgdprs747273828
ensemblrs747273828
gopubmedrs747273828
geneviewrs747273828
scholarrs747273828
googlers747273828
pharmgkbrs747273828
gwascentralrs747273828
openSNPrs747273828
23andMers747273828
23andMe allrs747273828
SNP Nexus

SNPshotrs747273828
SNPdbers747273828
MSV3drs747273828
GWAS Ctlgrs747273828
Max Magnitude0
ClinVar
Risk rs747273828(A,C;A,C)
Alt rs747273828(A,C;A,C)
Reference rs747273828(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40699897G>A; NC_000015.9:g.40699897G>C
CLNSRC
CLNACC RCV000185979.1, RCV000185980.1,