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rs797044864

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044864(A;A)
Make rs797044864(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position48478081
GeneFTSJ1
is asnp
is mentioned by
dbSNPrs797044864
ebirs797044864
HLIrs797044864
Exacrs797044864
Varsomers797044864
Maprs797044864
PheGenIrs797044864
hapmaprs797044864
1000 genomesrs797044864
hgdprs797044864
ensemblrs797044864
gopubmedrs797044864
geneviewrs797044864
scholarrs797044864
googlers797044864
pharmgkbrs797044864
gwascentralrs797044864
openSNPrs797044864
23andMers797044864
23andMe allrs797044864
SNP Nexus

SNPshotrs797044864
SNPdbers797044864
MSV3drs797044864
GWAS Ctlgrs797044864
Max Magnitude0
ClinVar
Risk rs797044864(A;A)
Alt rs797044864(A;A)
Reference rs797044864(T;T)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FTSJ1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.48336469T>A
CLNSRC
CLNACC RCV000190669.1,