Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044535

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044535(C;T)
Make rs797044535(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235802998
GeneLYST
is asnp
is mentioned by
dbSNPrs797044535
ebirs797044535
HLIrs797044535
Exacrs797044535
Varsomers797044535
Maprs797044535
PheGenIrs797044535
hapmaprs797044535
1000 genomesrs797044535
hgdprs797044535
ensemblrs797044535
gopubmedrs797044535
geneviewrs797044535
scholarrs797044535
googlers797044535
pharmgkbrs797044535
gwascentralrs797044535
openSNPrs797044535
23andMers797044535
23andMe allrs797044535
SNP Nexus

SNPshotrs797044535
SNPdbers797044535
MSV3drs797044535
GWAS Ctlgrs797044535
Max Magnitude0
ClinVar
Risk rs797044535(T;T)
Alt rs797044535(T;T)
Reference rs797044535(C;C)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235966298G>A
CLNSRC
CLNACC RCV000192044.1,