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

rs748659198

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748659198(C;T)
Make rs748659198(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position235759159
GeneLYST
is asnp
is mentioned by
dbSNPrs748659198
ebirs748659198
HLIrs748659198
Exacrs748659198
Varsomers748659198
Maprs748659198
PheGenIrs748659198
hapmaprs748659198
1000 genomesrs748659198
hgdprs748659198
ensemblrs748659198
gopubmedrs748659198
geneviewrs748659198
scholarrs748659198
googlers748659198
pharmgkbrs748659198
gwascentralrs748659198
openSNPrs748659198
23andMers748659198
23andMe allrs748659198
SNP Nexus

SNPshotrs748659198
SNPdbers748659198
MSV3drs748659198
GWAS Ctlgrs748659198
Max Magnitude0
ClinVar
Risk rs748659198(A,T;A,T)
Alt rs748659198(A,T;A,T)
Reference rs748659198(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LYST
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.235922459C>A
CLNSRC
CLNACC RCV000171169.1,