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rs398123623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGGTGAGC;AGGTGAGC) 0 common in clinvar
Make rs398123623(-;-)
Make rs398123623(-;AGGTGAGC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154349643
GeneFLNA
is asnp
is mentioned by
dbSNPrs398123623
ebirs398123623
HLIrs398123623
Exacrs398123623
Varsomers398123623
Maprs398123623
PheGenIrs398123623
hapmaprs398123623
1000 genomesrs398123623
hgdprs398123623
ensemblrs398123623
gopubmedrs398123623
geneviewrs398123623
scholarrs398123623
googlers398123623
pharmgkbrs398123623
gwascentralrs398123623
openSNPrs398123623
23andMers398123623
23andMe allrs398123623
SNP Nexus

SNPshotrs398123623
SNPdbers398123623
MSV3drs398123623
GWAS Ctlgrs398123623
Max Magnitude0
ClinVar
Risk rs398123623(;)
Alt rs398123623(;)
Reference rs398123623(AGGTGAGC;AGGTGAGC)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.11:g.154349643_154349650delGCTCACCT
CLNSRC ClinVar
CLNACC RCV000079710.1,