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rs1057518435

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518435(A;T)
Make rs1057518435(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position43182234
GeneHGSNAT
is asnp
is mentioned by
dbSNPrs1057518435
dbSNP (old)rs1057518435
ClinGenrs1057518435
ebirs1057518435
HLIrs1057518435
Exacrs1057518435
Gnomadrs1057518435
Varsomers1057518435
Maprs1057518435
PheGenIrs1057518435
Biobankrs1057518435
1000 genomesrs1057518435
hgdprs1057518435
ensemblrs1057518435
gopubmedrs1057518435
geneviewrs1057518435
scholarrs1057518435
googlers1057518435
pharmgkbrs1057518435
gwascentralrs1057518435
openSNPrs1057518435
23andMers1057518435
23andMe allrs1057518435
SNPshotrs1057518435
SNPdbers1057518435
MSV3drs1057518435
GWAS Ctlgrs1057518435
Max Magnitude0
ClinVar
Risk rs1057518435(T;T)
Alt rs1057518435(T;T)
Reference Rs1057518435(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HGSNAT
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.43037377A>T
CLNSRC
CLNACC RCV000414027.1,