Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518109(C;G)
Make rs1057518109(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154367729
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057518109
dbSNP (old)rs1057518109
ClinGenrs1057518109
ebirs1057518109
HLIrs1057518109
Exacrs1057518109
Gnomadrs1057518109
Varsomers1057518109
LitVarrs1057518109
Maprs1057518109
PheGenIrs1057518109
Biobankrs1057518109
1000 genomesrs1057518109
hgdprs1057518109
ensemblrs1057518109
gopubmedrs1057518109
geneviewrs1057518109
scholarrs1057518109
googlers1057518109
pharmgkbrs1057518109
gwascentralrs1057518109
openSNPrs1057518109
23andMers1057518109
23andMe allrs1057518109
SNPshotrs1057518109
SNPdbers1057518109
MSV3drs1057518109
GWAS Ctlgrs1057518109
Max Magnitude0
ClinVar
Risk rs1057518109(G;G)
Alt rs1057518109(G;G)
Reference Rs1057518109(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153596097G>C
CLNSRC
CLNACC RCV000412807.1,