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rs202182978

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202182978(C;T)
Make rs202182978(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89100709
GeneACSF3
is asnp
is mentioned by
dbSNPrs202182978
ebirs202182978
HLIrs202182978
Exacrs202182978
Varsomers202182978
Maprs202182978
PheGenIrs202182978
hapmaprs202182978
1000 genomesrs202182978
hgdprs202182978
ensemblrs202182978
gopubmedrs202182978
geneviewrs202182978
scholarrs202182978
googlers202182978
pharmgkbrs202182978
gwascentralrs202182978
openSNPrs202182978
23andMers202182978
23andMe allrs202182978
SNP Nexus

SNPshotrs202182978
SNPdbers202182978
MSV3drs202182978
GWAS Ctlgrs202182978
Max Magnitude0
ClinVar
Risk rs202182978(A,T;A,T)
Alt rs202182978(A,T;A,T)
Reference rs202182978(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ACSF3
CLNDBN not specified not provided
Reversed 0
HGVS NC_000016.9:g.89167117C>T
CLNSRC
CLNACC RCV000185753.1, RCV000224144.1,