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rs730882230

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882230(A;A)
Make rs730882230(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position128408688
GeneFBN2
is asnp
is mentioned by
dbSNPrs730882230
ebirs730882230
HLIrs730882230
Exacrs730882230
Varsomers730882230
Maprs730882230
PheGenIrs730882230
hapmaprs730882230
1000 genomesrs730882230
hgdprs730882230
ensemblrs730882230
gopubmedrs730882230
geneviewrs730882230
scholarrs730882230
googlers730882230
pharmgkbrs730882230
gwascentralrs730882230
openSNPrs730882230
23andMers730882230
23andMe allrs730882230
SNP Nexus

SNPshotrs730882230
SNPdbers730882230
MSV3drs730882230
GWAS Ctlgrs730882230
Max Magnitude0
ClinVar
Risk rs730882230(A;A)
Alt rs730882230(A;A)
Reference rs730882230(G;G)
Significance Probable-Pathogenic
Disease Cerebral ischemia Fetal akinesia sequence Neonatal death
Variation info
Gene FBN2
CLNDBN Cerebral ischemia Fetal akinesia sequence Neonatal death
Reversed 1
HGVS NC_000005.9:g.127744381C>T
CLNSRC
CLNACC RCV000162150.1,