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rs1017700992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position53314796
GeneAAAS
is asnp
is mentioned by
dbSNPrs1017700992
dbSNP (old)rs1017700992
ClinGenrs1017700992
ebirs1017700992
HLIrs1017700992
Exacrs1017700992
Gnomadrs1017700992
Varsomers1017700992
Maprs1017700992
PheGenIrs1017700992
Biobankrs1017700992
1000 genomesrs1017700992
hgdprs1017700992
ensemblrs1017700992
gopubmedrs1017700992
geneviewrs1017700992
scholarrs1017700992
googlers1017700992
pharmgkbrs1017700992
gwascentralrs1017700992
openSNPrs1017700992
23andMers1017700992
23andMe allrs1017700992
SNPshotrs1017700992
SNPdbers1017700992
MSV3drs1017700992
GWAS Ctlgrs1017700992
Max Magnitude0
ClinVar
Risk rs1017700992(A;A)
Alt rs1017700992(A;A)
Reference Rs1017700992(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AAAS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.53708580G>T
CLNSRC
CLNACC RCV000413311.1,