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rs387907266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907266(G;T)
Make rs387907266(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4945970
GenePFN1
is asnp
is mentioned by
dbSNPrs387907266
ebirs387907266
HLIrs387907266
Exacrs387907266
Varsomers387907266
Maprs387907266
PheGenIrs387907266
hapmaprs387907266
1000 genomesrs387907266
hgdprs387907266
ensemblrs387907266
gopubmedrs387907266
geneviewrs387907266
scholarrs387907266
googlers387907266
pharmgkbrs387907266
gwascentralrs387907266
openSNPrs387907266
23andMers387907266
23andMe allrs387907266
SNP Nexus

SNPshotrs387907266
SNPdbers387907266
MSV3drs387907266
GWAS Ctlgrs387907266
Max Magnitude0
ClinVar
Risk rs387907266(T;T)
Alt rs387907266(T;T)
Reference rs387907266(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis 18
Variation info
Gene PFN1
CLNDBN Amyotrophic lateral sclerosis 18
Reversed 1
HGVS NC_000017.10:g.4849265C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030696.17,