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rs754043007

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754043007(A;A)
Make rs754043007(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position97853097
GeneASNS
is asnp
is mentioned by
dbSNPrs754043007
ebirs754043007
HLIrs754043007
Exacrs754043007
Varsomers754043007
Maprs754043007
PheGenIrs754043007
hapmaprs754043007
1000 genomesrs754043007
hgdprs754043007
ensemblrs754043007
gopubmedrs754043007
geneviewrs754043007
scholarrs754043007
googlers754043007
pharmgkbrs754043007
gwascentralrs754043007
openSNPrs754043007
23andMers754043007
23andMe allrs754043007
SNP Nexus

SNPshotrs754043007
SNPdbers754043007
MSV3drs754043007
GWAS Ctlgrs754043007
Max Magnitude0
ClinVar
Risk rs754043007(A;A)
Alt rs754043007(A;A)
Reference rs754043007(G;G)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene ASNS
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000007.13:g.97482409G>A
CLNSRC
CLNACC RCV000201411.1,