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rs387907264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907264(G;G)
Make rs387907264(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4946742
GenePFN1
is asnp
is mentioned by
dbSNPrs387907264
ebirs387907264
HLIrs387907264
Exacrs387907264
Varsomers387907264
Maprs387907264
PheGenIrs387907264
hapmaprs387907264
1000 genomesrs387907264
hgdprs387907264
ensemblrs387907264
gopubmedrs387907264
geneviewrs387907264
scholarrs387907264
googlers387907264
pharmgkbrs387907264
gwascentralrs387907264
openSNPrs387907264
23andMers387907264
23andMe allrs387907264
SNP Nexus

SNPshotrs387907264
SNPdbers387907264
MSV3drs387907264
GWAS Ctlgrs387907264
Max Magnitude0
ClinVar
Risk rs387907264(G;G)
Alt rs387907264(G;G)
Reference rs387907264(T;T)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis 18
Variation info
Gene PFN1
CLNDBN Amyotrophic lateral sclerosis 18
Reversed 1
HGVS NC_000017.10:g.4850037A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030694.24,