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rs80338661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTATTAG;CTATTAG) 0 common in clinvar
Make rs80338661(-;-)
Make rs80338661(-;CTATTAG)
ReferenceGRCh38 38.1/141
Chromosome1
Position235755641
GeneLYST
is asnp
is mentioned by
dbSNPrs80338661
ebirs80338661
HLIrs80338661
Exacrs80338661
Varsomers80338661
Maprs80338661
PheGenIrs80338661
hapmaprs80338661
1000 genomesrs80338661
hgdprs80338661
ensemblrs80338661
gopubmedrs80338661
geneviewrs80338661
scholarrs80338661
googlers80338661
pharmgkbrs80338661
gwascentralrs80338661
openSNPrs80338661
23andMers80338661
23andMe allrs80338661
SNP Nexus

SNPshotrs80338661
SNPdbers80338661
MSV3drs80338661
GWAS Ctlgrs80338661
Max Magnitude0
ClinVar
Risk rs80338661(;)
Alt rs80338661(;)
Reference rs80338661(CTATTAG;CTATTAG)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235918941_235918947delCTAATAG
CLNSRC ClinVar GeneReviews
CLNACC RCV000055740.1,