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rs797044542

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044542(A;A)
Make rs797044542(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235664487
GeneLYST
is asnp
is mentioned by
dbSNPrs797044542
ebirs797044542
HLIrs797044542
Exacrs797044542
Varsomers797044542
Maprs797044542
PheGenIrs797044542
hapmaprs797044542
1000 genomesrs797044542
hgdprs797044542
ensemblrs797044542
gopubmedrs797044542
geneviewrs797044542
scholarrs797044542
googlers797044542
pharmgkbrs797044542
gwascentralrs797044542
openSNPrs797044542
23andMers797044542
23andMe allrs797044542
SNP Nexus

SNPshotrs797044542
SNPdbers797044542
MSV3drs797044542
GWAS Ctlgrs797044542
Max Magnitude0
ClinVar
Risk rs797044542(A;A)
Alt rs797044542(A;A)
Reference rs797044542(G;G)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235827787C>T
CLNSRC
CLNACC RCV000192052.1,