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rs17679127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17679127(A;G)
Make rs17679127(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position103423754
GeneMARK3
is asnp
is mentioned by
dbSNPrs17679127
ebirs17679127
HLIrs17679127
Exacrs17679127
Varsomers17679127
Maprs17679127
PheGenIrs17679127
hapmaprs17679127
1000 genomesrs17679127
hgdprs17679127
ensemblrs17679127
gopubmedrs17679127
geneviewrs17679127
scholarrs17679127
googlers17679127
pharmgkbrs17679127
gwascentralrs17679127
openSNPrs17679127
23andMers17679127
23andMe allrs17679127
SNP Nexus

SNPshotrs17679127
SNPdbers17679127
MSV3drs17679127
GWAS Ctlgrs17679127
GMAF0.07484
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20697106OA-icon.png] Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32
OMIM158600
Desc
Variant
Relatedalso