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rs797044541

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044541(G;T)
Make rs797044541(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235664558
GeneLYST
is asnp
is mentioned by
dbSNPrs797044541
ClinGenrs797044541
ebirs797044541
HLIrs797044541
Exacrs797044541
Varsomers797044541
Maprs797044541
PheGenIrs797044541
hapmaprs797044541
1000 genomesrs797044541
hgdprs797044541
ensemblrs797044541
gopubmedrs797044541
geneviewrs797044541
scholarrs797044541
googlers797044541
pharmgkbrs797044541
gwascentralrs797044541
openSNPrs797044541
23andMers797044541
23andMe allrs797044541
SNP Nexus

SNPshotrs797044541
SNPdbers797044541
MSV3drs797044541
GWAS Ctlgrs797044541
Max Magnitude0
ClinVar
Risk rs797044541(T;T)
Alt rs797044541(T;T)
Reference Rs797044541(G;G)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235827858C>A
CLNSRC
CLNACC RCV000192051.1,