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rs781134478

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs781134478(G;G)
Make rs781134478(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position30904756
GeneFAN1
is asnp
is mentioned by
dbSNPrs781134478
ebirs781134478
HLIrs781134478
Exacrs781134478
Varsomers781134478
Maprs781134478
PheGenIrs781134478
hapmaprs781134478
1000 genomesrs781134478
hgdprs781134478
ensemblrs781134478
gopubmedrs781134478
geneviewrs781134478
scholarrs781134478
googlers781134478
pharmgkbrs781134478
gwascentralrs781134478
openSNPrs781134478
23andMers781134478
23andMe allrs781134478
SNP Nexus

SNPshotrs781134478
SNPdbers781134478
MSV3drs781134478
GWAS Ctlgrs781134478
Max Magnitude0
ClinVar
Risk rs781134478(G;G)
Alt rs781134478(G;G)
Reference rs781134478(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FAN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.31196959T>G
CLNSRC
CLNACC RCV000171228.1,