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rs797044538

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044538(C;G)
Make rs797044538(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235744148
GeneLYST
is asnp
is mentioned by
dbSNPrs797044538
ebirs797044538
HLIrs797044538
Exacrs797044538
Varsomers797044538
Maprs797044538
PheGenIrs797044538
hapmaprs797044538
1000 genomesrs797044538
hgdprs797044538
ensemblrs797044538
gopubmedrs797044538
geneviewrs797044538
scholarrs797044538
googlers797044538
pharmgkbrs797044538
gwascentralrs797044538
openSNPrs797044538
23andMers797044538
23andMe allrs797044538
SNP Nexus

SNPshotrs797044538
SNPdbers797044538
MSV3drs797044538
GWAS Ctlgrs797044538
Max Magnitude0
ClinVar
Risk rs797044538(G;G)
Alt rs797044538(G;G)
Reference rs797044538(C;C)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 1
HGVS NC_000001.10:g.235907448G>C
CLNSRC
CLNACC RCV000192048.1,