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rs80338655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80338655(A;A)
Make rs80338655(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position235791881
GeneLYST
is asnp
is mentioned by
dbSNPrs80338655
ebirs80338655
HLIrs80338655
Exacrs80338655
Varsomers80338655
Maprs80338655
PheGenIrs80338655
hapmaprs80338655
1000 genomesrs80338655
hgdprs80338655
ensemblrs80338655
gopubmedrs80338655
geneviewrs80338655
scholarrs80338655
googlers80338655
pharmgkbrs80338655
gwascentralrs80338655
openSNPrs80338655
23andMers80338655
23andMe allrs80338655
SNP Nexus

SNPshotrs80338655
SNPdbers80338655
MSV3drs80338655
GWAS Ctlgrs80338655
Max Magnitude0
ClinVar
Risk rs80338655(A;A)
Alt rs80338655(A;A)
Reference rs80338655(C;C)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235955181G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055734.1,