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rs387907265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907265(C;C)
Make rs387907265(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4945982
GenePFN1
is asnp
is mentioned by
dbSNPrs387907265
ebirs387907265
HLIrs387907265
Exacrs387907265
Varsomers387907265
Maprs387907265
PheGenIrs387907265
hapmaprs387907265
1000 genomesrs387907265
hgdprs387907265
ensemblrs387907265
gopubmedrs387907265
geneviewrs387907265
scholarrs387907265
googlers387907265
pharmgkbrs387907265
gwascentralrs387907265
openSNPrs387907265
23andMers387907265
23andMe allrs387907265
SNP Nexus

SNPshotrs387907265
SNPdbers387907265
MSV3drs387907265
GWAS Ctlgrs387907265
Max Magnitude0
ClinVar
Risk rs387907265(C;C)
Alt rs387907265(C;C)
Reference rs387907265(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.4849277A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000030695.17,