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rs863223632

From SNPedia

Orientationminus
Make rs863223632(-;-)
Make rs863223632(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154359790
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223632
ebirs863223632
HLIrs863223632
Exacrs863223632
Varsomers863223632
Maprs863223632
PheGenIrs863223632
hapmaprs863223632
1000 genomesrs863223632
hgdprs863223632
ensemblrs863223632
gopubmedrs863223632
geneviewrs863223632
scholarrs863223632
googlers863223632
pharmgkbrs863223632
gwascentralrs863223632
openSNPrs863223632
23andMers863223632
23andMe allrs863223632
SNP Nexus

SNPshotrs863223632
SNPdbers863223632
MSV3drs863223632
GWAS Ctlgrs863223632
Max Magnitude
ClinVar
Risk rs863223632(;)
Alt rs863223632(;)
Reference rs863223632(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153588158delG
CLNSRC
CLNACC RCV000199592.2,