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rs398122521

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398122521(-;-)
Make rs398122521(-;TC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154371229
GeneFLNA
is asnp
is mentioned by
dbSNPrs398122521
ebirs398122521
HLIrs398122521
Exacrs398122521
Varsomers398122521
Maprs398122521
PheGenIrs398122521
hapmaprs398122521
1000 genomesrs398122521
hgdprs398122521
ensemblrs398122521
gopubmedrs398122521
geneviewrs398122521
scholarrs398122521
googlers398122521
pharmgkbrs398122521
gwascentralrs398122521
openSNPrs398122521
23andMers398122521
23andMe allrs398122521
SNP Nexus

SNPshotrs398122521
SNPdbers398122521
MSV3drs398122521
GWAS Ctlgrs398122521
Max Magnitude0
ClinVar
Risk rs398122521(;)
Alt rs398122521(;)
Reference rs398122521(TC;TC)
Significance Pathogenic
Disease Congenital short bowel syndrome
Variation info
Gene FLNA
CLNDBN Congenital short bowel syndrome, X-linked
Reversed 1
HGVS NC_000023.10:g.153599597_153599598delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000043474.26,