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rs863225287

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225287(G;T)
Make rs863225287(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position44711614
GeneB2M, PATL2
is asnp
is mentioned by
dbSNPrs863225287
ebirs863225287
HLIrs863225287
Exacrs863225287
Varsomers863225287
Maprs863225287
PheGenIrs863225287
hapmaprs863225287
1000 genomesrs863225287
hgdprs863225287
ensemblrs863225287
gopubmedrs863225287
geneviewrs863225287
scholarrs863225287
googlers863225287
pharmgkbrs863225287
gwascentralrs863225287
openSNPrs863225287
23andMers863225287
23andMe allrs863225287
SNP Nexus

SNPshotrs863225287
SNPdbers863225287
MSV3drs863225287
GWAS Ctlgrs863225287
Max Magnitude0
ClinVar
Risk rs863225287(T;T)
Alt rs863225287(T;T)
Reference rs863225287(G;G)
Significance Pathogenic
Disease Hypoproteinemia
Variation info
Gene B2M
CLNDBN Hypoproteinemia, hypercatabolic
Reversed 0
HGVS NC_000015.9:g.45003812G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000201934.2,