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rs137853316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853316(G;T)
Make rs137853316(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154354860
GeneFLNA
is asnp
is mentioned by
dbSNPrs137853316
ebirs137853316
HLIrs137853316
Exacrs137853316
Varsomers137853316
Maprs137853316
PheGenIrs137853316
hapmaprs137853316
1000 genomesrs137853316
hgdprs137853316
ensemblrs137853316
gopubmedrs137853316
geneviewrs137853316
scholarrs137853316
googlers137853316
pharmgkbrs137853316
gwascentralrs137853316
openSNPrs137853316
23andMers137853316
23andMe allrs137853316
SNP Nexus

SNPshotrs137853316
SNPdbers137853316
MSV3drs137853316
GWAS Ctlgrs137853316
Max Magnitude0
OMIM300017
Desc
Variant0022
Relatedalso
ClinVar
Risk rs137853316(T;T)
Alt rs137853316(T;T)
Reference rs137853316(G;G)
Significance Pathogenic
Disease Otopalatodigital spectrum disorder
Variation info
Gene FLNA
CLNDBN Otopalatodigital spectrum disorder
Reversed 1
HGVS NC_000023.10:g.153583228C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012534.22,