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

rs1057518223

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518223(A;A)
Make rs1057518223(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154358356
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057518223
dbSNP (old)rs1057518223
ClinGenrs1057518223
ebirs1057518223
HLIrs1057518223
Exacrs1057518223
Gnomadrs1057518223
Varsomers1057518223
Maprs1057518223
PheGenIrs1057518223
Biobankrs1057518223
1000 genomesrs1057518223
hgdprs1057518223
ensemblrs1057518223
gopubmedrs1057518223
geneviewrs1057518223
scholarrs1057518223
googlers1057518223
pharmgkbrs1057518223
gwascentralrs1057518223
openSNPrs1057518223
23andMers1057518223
23andMe allrs1057518223
SNPshotrs1057518223
SNPdbers1057518223
MSV3drs1057518223
GWAS Ctlgrs1057518223
Max Magnitude0
ClinVar
Risk rs1057518223(A;A)
Alt rs1057518223(A;A)
Reference Rs1057518223(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153586724C>T
CLNSRC
CLNACC RCV000414514.1,