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rs201954387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201954387(A;A)
Make rs201954387(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89146044
GeneACSF3
is asnp
is mentioned by
dbSNPrs201954387
dbSNP (classic)rs201954387
ClinGenrs201954387
ebirs201954387
HLIrs201954387
Exacrs201954387
Gnomadrs201954387
Varsomers201954387
LitVarrs201954387
Maprs201954387
PheGenIrs201954387
Biobankrs201954387
1000 genomesrs201954387
hgdprs201954387
ensemblrs201954387
geneviewrs201954387
scholarrs201954387
googlers201954387
pharmgkbrs201954387
gwascentralrs201954387
openSNPrs201954387
23andMers201954387
23andMe allrs201954387
SNPshotrs201954387
SNPdbers201954387
MSV3drs201954387
GWAS Ctlgrs201954387
Max Magnitude0
ClinVar
Risk rs201954387(A;A)
Alt rs201954387(A;A)
Reference Rs201954387(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89212452G>A
CLNSRC
CLNACC RCV000426583.1,