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rs878853009

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853009(C;T)
Make rs878853009(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position78534471
GeneFRAS1
is asnp
is mentioned by
dbSNPrs878853009
ebirs878853009
HLIrs878853009
Exacrs878853009
Varsomers878853009
Maprs878853009
PheGenIrs878853009
hapmaprs878853009
1000 genomesrs878853009
hgdprs878853009
ensemblrs878853009
gopubmedrs878853009
geneviewrs878853009
scholarrs878853009
googlers878853009
pharmgkbrs878853009
gwascentralrs878853009
openSNPrs878853009
23andMers878853009
23andMe allrs878853009
SNP Nexus

SNPshotrs878853009
SNPdbers878853009
MSV3drs878853009
GWAS Ctlgrs878853009
Max Magnitude0
ClinVar
Risk rs878853009(T;T)
Alt rs878853009(T;T)
Reference rs878853009(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FRAS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.79455625C>T
CLNSRC
CLNACC RCV000224396.1,