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

rs878854368

From SNPedia

Orientationminus
Geno Mag Summary
(TCAA;TCAA) 0 common in clinvar
Make rs878854368(-;-)
Make rs878854368(-;TCAA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position151646140
GeneNEB
is asnp
is mentioned by
dbSNPrs878854368
ebirs878854368
HLIrs878854368
Exacrs878854368
Varsomers878854368
Maprs878854368
PheGenIrs878854368
hapmaprs878854368
1000 genomesrs878854368
hgdprs878854368
ensemblrs878854368
gopubmedrs878854368
geneviewrs878854368
scholarrs878854368
googlers878854368
pharmgkbrs878854368
gwascentralrs878854368
openSNPrs878854368
23andMers878854368
23andMe allrs878854368
SNP Nexus

SNPshotrs878854368
SNPdbers878854368
MSV3drs878854368
GWAS Ctlgrs878854368
Max Magnitude0
ClinVar
Risk rs878854368(;)
Alt rs878854368(;)
Reference rs878854368(TCAA;TCAA)
Significance Probable-Pathogenic
Disease Nemaline myopathy 2
Variation info
Gene NEB
CLNDBN Nemaline myopathy 2
Reversed 1
HGVS NC_000002.11:g.152502654_152502657delTTGA
CLNSRC
CLNACC RCV000227541.1,