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rs199751308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199751308(A;G)
Make rs199751308(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130489423
GeneASS1
is asnp
is mentioned by
dbSNPrs199751308
dbSNP (classic)rs199751308
ClinGenrs199751308
ebirs199751308
HLIrs199751308
Exacrs199751308
Gnomadrs199751308
Varsomers199751308
LitVarrs199751308
Maprs199751308
PheGenIrs199751308
Biobankrs199751308
1000 genomesrs199751308
hgdprs199751308
ensemblrs199751308
geneviewrs199751308
scholarrs199751308
googlers199751308
pharmgkbrs199751308
gwascentralrs199751308
openSNPrs199751308
23andMers199751308
23andMe allrs199751308
SNPshotrs199751308
SNPdbers199751308
MSV3drs199751308
GWAS Ctlgrs199751308
Max Magnitude0
ClinVar
Risk rs199751308(G;G)
Alt rs199751308(G;G)
Reference Rs199751308(A;A)
Significance Probable-Pathogenic
Disease Citrullinemia type I not provided
Variation info
Gene ASS1
CLNDBN Citrullinemia type I not provided
Reversed 0
HGVS NC_000009.11:g.133364810A>G
CLNSRC
CLNACC RCV000286574.1, RCV000413247.1,