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rs878854600

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854600(C;T)
Make rs878854600(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position23834262
GeneDERL3, SMARCB1
is asnp
is mentioned by
dbSNPrs878854600
ebirs878854600
HLIrs878854600
Exacrs878854600
Varsomers878854600
Maprs878854600
PheGenIrs878854600
hapmaprs878854600
1000 genomesrs878854600
hgdprs878854600
ensemblrs878854600
gopubmedrs878854600
geneviewrs878854600
scholarrs878854600
googlers878854600
pharmgkbrs878854600
gwascentralrs878854600
openSNPrs878854600
23andMers878854600
23andMe allrs878854600
SNP Nexus

SNPshotrs878854600
SNPdbers878854600
MSV3drs878854600
GWAS Ctlgrs878854600
Max Magnitude0
ClinVar
Risk rs878854600(T;T)
Alt rs878854600(T;T)
Reference rs878854600(C;C)
Significance Pathogenic
Disease Rhabdoid tumor predisposition syndrome 1 Schwannomatosis
Variation info
Gene DERL3 SMARCB1
CLNDBN Rhabdoid tumor predisposition syndrome 1 Schwannomatosis
Reversed 0
HGVS NC_000022.10:g.24176449C>T
CLNSRC
CLNACC RCV000231611.1,