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rs137853065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853065(C;C)
Make rs137853065(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38138978
GeneACAA1, MYD88
is asnp
is mentioned by
dbSNPrs137853065
ebirs137853065
HLIrs137853065
Exacrs137853065
Varsomers137853065
Maprs137853065
PheGenIrs137853065
hapmaprs137853065
1000 genomesrs137853065
hgdprs137853065
ensemblrs137853065
gopubmedrs137853065
geneviewrs137853065
scholarrs137853065
googlers137853065
pharmgkbrs137853065
gwascentralrs137853065
openSNPrs137853065
23andMers137853065
23andMe allrs137853065
SNP Nexus

SNPshotrs137853065
SNPdbers137853065
MSV3drs137853065
GWAS Ctlgrs137853065
Max Magnitude0
OMIM602170
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853065(C;C)
Alt rs137853065(C;C)
Reference rs137853065(T;T)
Significance Pathogenic
Disease Myd88 deficiency
Variation info
Gene ACAA1 MYD88
CLNDBN Myd88 deficiency
Reversed 0
HGVS NC_000003.11:g.38180469T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007925.4,