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rs757905943

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757905943(A;A)
Make rs757905943(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89101029
GeneACSF3
is asnp
is mentioned by
dbSNPrs757905943
ebirs757905943
HLIrs757905943
Exacrs757905943
Varsomers757905943
Maprs757905943
PheGenIrs757905943
hapmaprs757905943
1000 genomesrs757905943
hgdprs757905943
ensemblrs757905943
gopubmedrs757905943
geneviewrs757905943
scholarrs757905943
googlers757905943
pharmgkbrs757905943
gwascentralrs757905943
openSNPrs757905943
23andMers757905943
23andMe allrs757905943
SNP Nexus

SNPshotrs757905943
SNPdbers757905943
MSV3drs757905943
GWAS Ctlgrs757905943
Max Magnitude0
ClinVar
Risk rs757905943(A;A)
Alt rs757905943(A;A)
Reference rs757905943(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89167437G>A
CLNSRC
CLNACC RCV000185754.1,