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rs121908898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908898(G;T)
Make rs121908898(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position58146043
GeneFLNB
is asnp
is mentioned by
dbSNPrs121908898
ebirs121908898
HLIrs121908898
Exacrs121908898
Varsomers121908898
Maprs121908898
PheGenIrs121908898
hapmaprs121908898
1000 genomesrs121908898
hgdprs121908898
ensemblrs121908898
gopubmedrs121908898
geneviewrs121908898
scholarrs121908898
googlers121908898
pharmgkbrs121908898
gwascentralrs121908898
openSNPrs121908898
23andMers121908898
23andMe allrs121908898
SNP Nexus

SNPshotrs121908898
SNPdbers121908898
MSV3drs121908898
GWAS Ctlgrs121908898
Max Magnitude0
OMIM603381
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121908898(T;T)
Alt rs121908898(T;T)
Reference rs121908898(G;G)
Significance Pathogenic
Disease Spondylocarpotarsal synostosis syndrome
Variation info
Gene FLNB
CLNDBN Spondylocarpotarsal synostosis syndrome
Reversed 0
HGVS NC_000003.11:g.58131770G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006777.2,