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rs137853064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853064(C;T)
Make rs137853064(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38140510
GeneMYD88
is asnp
is mentioned by
dbSNPrs137853064
ebirs137853064
HLIrs137853064
Exacrs137853064
Varsomers137853064
Maprs137853064
PheGenIrs137853064
hapmaprs137853064
1000 genomesrs137853064
hgdprs137853064
ensemblrs137853064
gopubmedrs137853064
geneviewrs137853064
scholarrs137853064
googlers137853064
pharmgkbrs137853064
gwascentralrs137853064
openSNPrs137853064
23andMers137853064
23andMe allrs137853064
SNP Nexus

SNPshotrs137853064
SNPdbers137853064
MSV3drs137853064
GWAS Ctlgrs137853064
Max Magnitude0
OMIM602170
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853064(T;T)
Alt rs137853064(T;T)
Reference rs137853064(C;C)
Significance Pathogenic
Disease Myd88 deficiency
Variation info
Gene MYD88
CLNDBN Myd88 deficiency
Reversed 0
HGVS NC_000003.11:g.38182001C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007924.3,