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rs121908897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908897(C;T)
Make rs121908897(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position58148771
GeneFLNB
is asnp
is mentioned by
dbSNPrs121908897
ebirs121908897
HLIrs121908897
Exacrs121908897
Varsomers121908897
Maprs121908897
PheGenIrs121908897
hapmaprs121908897
1000 genomesrs121908897
hgdprs121908897
ensemblrs121908897
gopubmedrs121908897
geneviewrs121908897
scholarrs121908897
googlers121908897
pharmgkbrs121908897
gwascentralrs121908897
openSNPrs121908897
23andMers121908897
23andMe allrs121908897
SNP Nexus

SNPshotrs121908897
SNPdbers121908897
MSV3drs121908897
GWAS Ctlgrs121908897
Max Magnitude0
OMIM603381
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908897(T;T)
Alt rs121908897(T;T)
Reference rs121908897(C;C)
Significance Pathogenic
Disease Spondylocarpotarsal synostosis syndrome
Variation info
Gene FLNB
CLNDBN Spondylocarpotarsal synostosis syndrome
Reversed 0
HGVS NC_000003.11:g.58134498C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006776.2,