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rs751298577

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751298577(G;T)
Make rs751298577(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position115587074
GeneTRPS1
is asnp
is mentioned by
dbSNPrs751298577
ebirs751298577
HLIrs751298577
Exacrs751298577
Varsomers751298577
Maprs751298577
PheGenIrs751298577
hapmaprs751298577
1000 genomesrs751298577
hgdprs751298577
ensemblrs751298577
gopubmedrs751298577
geneviewrs751298577
scholarrs751298577
googlers751298577
pharmgkbrs751298577
gwascentralrs751298577
openSNPrs751298577
23andMers751298577
23andMe allrs751298577
SNP Nexus

SNPshotrs751298577
SNPdbers751298577
MSV3drs751298577
GWAS Ctlgrs751298577
Max Magnitude0
ClinVar
Risk rs751298577(A,T;A,T)
Alt rs751298577(A,T;A,T)
Reference rs751298577(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene TRPS1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.116599301G>A
CLNSRC
CLNACC RCV000190752.1,