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rs80338664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80338664(A;A)
Make rs80338664(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position235733859
GeneLYST
is asnp
is mentioned by
dbSNPrs80338664
ebirs80338664
HLIrs80338664
Exacrs80338664
Varsomers80338664
Maprs80338664
PheGenIrs80338664
hapmaprs80338664
1000 genomesrs80338664
hgdprs80338664
ensemblrs80338664
gopubmedrs80338664
geneviewrs80338664
scholarrs80338664
googlers80338664
pharmgkbrs80338664
gwascentralrs80338664
openSNPrs80338664
23andMers80338664
23andMe allrs80338664
SNP Nexus

SNPshotrs80338664
SNPdbers80338664
MSV3drs80338664
GWAS Ctlgrs80338664
Max Magnitude0
ClinVar
Risk rs80338664(A;A)
Alt rs80338664(A;A)
Reference rs80338664(G;G)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235897159C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055743.1,