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rs387907272

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907272(C;C)
Make rs387907272(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38141150
GeneMYD88
is asnp
is mentioned by
dbSNPrs387907272
ebirs387907272
HLIrs387907272
Exacrs387907272
Varsomers387907272
Maprs387907272
PheGenIrs387907272
hapmaprs387907272
1000 genomesrs387907272
hgdprs387907272
ensemblrs387907272
gopubmedrs387907272
geneviewrs387907272
scholarrs387907272
googlers387907272
pharmgkbrs387907272
gwascentralrs387907272
openSNPrs387907272
23andMers387907272
23andMe allrs387907272
SNP Nexus

SNPshotrs387907272
SNPdbers387907272
MSV3drs387907272
GWAS Ctlgrs387907272
Max Magnitude0
ClinVar
Risk rs387907272(C;C)
Alt rs387907272(C;C)
Reference rs387907272(T;T)
Significance Pathogenic
Disease Macroglobulinemia
Variation info
Gene MYD88
CLNDBN Macroglobulinemia, waldenstrom, somatic
Reversed 0
HGVS NC_000003.11:g.38182641T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030709.6,