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rs757222354

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757222354(A;A)
Make rs757222354(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position235775041
GeneLYST
is asnp
is mentioned by
dbSNPrs757222354
ebirs757222354
HLIrs757222354
Exacrs757222354
Varsomers757222354
Maprs757222354
PheGenIrs757222354
hapmaprs757222354
1000 genomesrs757222354
hgdprs757222354
ensemblrs757222354
gopubmedrs757222354
geneviewrs757222354
scholarrs757222354
googlers757222354
pharmgkbrs757222354
gwascentralrs757222354
openSNPrs757222354
23andMers757222354
23andMe allrs757222354
SNP Nexus

SNPshotrs757222354
SNPdbers757222354
MSV3drs757222354
GWAS Ctlgrs757222354
Max Magnitude0
ClinVar
Risk rs757222354(A,T;A,T)
Alt rs757222354(A,T;A,T)
Reference rs757222354(G;G)
Significance Pathogenic
Disease Chédiak-Higashi syndrome
Variation info
Gene LYST
CLNDBN Chédiak-Higashi syndrome
Reversed 0
HGVS NC_000001.10:g.235938341G>A
CLNSRC
CLNACC RCV000192046.1,