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rs752076094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs752076094(A;G)
Make rs752076094(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position31185175
GeneFUS
is asnp
is mentioned by
dbSNPrs752076094
dbSNP (classic)rs752076094
ClinGenrs752076094
ebirs752076094
HLIrs752076094
Exacrs752076094
Gnomadrs752076094
Varsomers752076094
LitVarrs752076094
Maprs752076094
PheGenIrs752076094
Biobankrs752076094
1000 genomesrs752076094
hgdprs752076094
ensemblrs752076094
geneviewrs752076094
scholarrs752076094
googlers752076094
pharmgkbrs752076094
gwascentralrs752076094
openSNPrs752076094
23andMers752076094
SNPshotrs752076094
SNPdbers752076094
MSV3drs752076094
GWAS Ctlgrs752076094
Max Magnitude0
ClinVar
Risk rs752076094(G;G)
Alt rs752076094(G;G)
Reference Rs752076094(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FUS
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.31196496A>G
CLNSRC
CLNACC RCV000489255.1,