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rs864309530

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309530(A;A)
Make rs864309530(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235806165
GeneLYST
is asnp
is mentioned by
dbSNPrs864309530
ebirs864309530
HLIrs864309530
Exacrs864309530
Varsomers864309530
Maprs864309530
PheGenIrs864309530
hapmaprs864309530
1000 genomesrs864309530
hgdprs864309530
ensemblrs864309530
gopubmedrs864309530
geneviewrs864309530
scholarrs864309530
googlers864309530
pharmgkbrs864309530
gwascentralrs864309530
openSNPrs864309530
23andMers864309530
23andMe allrs864309530
SNP Nexus

SNPshotrs864309530
SNPdbers864309530
MSV3drs864309530
GWAS Ctlgrs864309530
Max Magnitude0
ClinVar
Risk rs864309530(A;A)
Alt rs864309530(A;A)
Reference rs864309530(C;C)
Significance Probable-Pathogenic
Disease Recurrent infections
Variation info
Gene LYST
CLNDBN Recurrent infections
Reversed 1
HGVS NC_000001.10:g.235969465G>T
CLNSRC
CLNACC RCV000202612.1,