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rs370382601

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs370382601(A;G)
Make rs370382601(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89100682
GeneACSF3
is asnp
is mentioned by
dbSNPrs370382601
ebirs370382601
HLIrs370382601
Exacrs370382601
Varsomers370382601
Maprs370382601
PheGenIrs370382601
hapmaprs370382601
1000 genomesrs370382601
hgdprs370382601
ensemblrs370382601
gopubmedrs370382601
geneviewrs370382601
scholarrs370382601
googlers370382601
pharmgkbrs370382601
gwascentralrs370382601
openSNPrs370382601
23andMers370382601
23andMe allrs370382601
SNP Nexus

SNPshotrs370382601
SNPdbers370382601
MSV3drs370382601
GWAS Ctlgrs370382601
Max Magnitude0
ClinVar
Risk rs370382601(G;G)
Alt rs370382601(G;G)
Reference rs370382601(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89167090A>G
CLNSRC
CLNACC RCV000185752.1,