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rs1052352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1052352(C;T)
Make rs1052352(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31183958
GeneFUS
is asnp
is mentioned by
dbSNPrs1052352
dbSNP (old)rs1052352
ClinGenrs1052352
ebirs1052352
HLIrs1052352
Exacrs1052352
Gnomadrs1052352
Varsomers1052352
Maprs1052352
PheGenIrs1052352
Biobankrs1052352
1000 genomesrs1052352
hgdprs1052352
ensemblrs1052352
gopubmedrs1052352
geneviewrs1052352
scholarrs1052352
googlers1052352
pharmgkbrs1052352
gwascentralrs1052352
openSNPrs1052352
23andMers1052352
23andMe allrs1052352
SNP Nexus

SNPshotrs1052352
SNPdbers1052352
MSV3drs1052352
GWAS Ctlgrs1052352
GMAF0.4646
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20061612] FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration


ClinVar
Risk rs1052352(T;T)
Alt rs1052352(T;T)
Reference Rs1052352(C;C)
Significance Non-pathogenic
Disease not specified Amyotrophic Lateral Sclerosis
Variation info
Gene FUS
CLNDBN not specified Amyotrophic Lateral Sclerosis, Dominant
Reversed 0
HGVS NC_000016.9:g.31195279C>T
CLNSRC
CLNACC RCV000244413.1, RCV000277026.1,