Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517127

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517127(A;A)
Make rs1057517127(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130479801
GeneASS1
is asnp
is mentioned by
dbSNPrs1057517127
dbSNP (old)rs1057517127
ClinGenrs1057517127
ebirs1057517127
HLIrs1057517127
Exacrs1057517127
Gnomadrs1057517127
Varsomers1057517127
Maprs1057517127
PheGenIrs1057517127
Biobankrs1057517127
1000 genomesrs1057517127
hgdprs1057517127
ensemblrs1057517127
gopubmedrs1057517127
geneviewrs1057517127
scholarrs1057517127
googlers1057517127
pharmgkbrs1057517127
gwascentralrs1057517127
openSNPrs1057517127
23andMers1057517127
23andMe allrs1057517127
SNPshotrs1057517127
SNPdbers1057517127
MSV3drs1057517127
GWAS Ctlgrs1057517127
Max Magnitude0
ClinVar
Risk rs1057517127(A;A)
Alt rs1057517127(A;A)
Reference Rs1057517127(G;G)
Significance Probable-Pathogenic
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133355188G>A
CLNSRC
CLNACC RCV000410118.1,