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rs561367199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs561367199(A;A)
Make rs561367199(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66082920
GeneASL
is asnp
is mentioned by
dbSNPrs561367199
dbSNP (classic)rs561367199
ClinGenrs561367199
ebirs561367199
HLIrs561367199
Exacrs561367199
Gnomadrs561367199
Varsomers561367199
LitVarrs561367199
Maprs561367199
PheGenIrs561367199
Biobankrs561367199
1000 genomesrs561367199
hgdprs561367199
ensemblrs561367199
geneviewrs561367199
scholarrs561367199
googlers561367199
pharmgkbrs561367199
gwascentralrs561367199
openSNPrs561367199
23andMers561367199
23andMe allrs561367199
SNPshotrs561367199
SNPdbers561367199
MSV3drs561367199
GWAS Ctlgrs561367199
Max Magnitude0
ClinVar
Risk rs561367199(A;A)
Alt rs561367199(A;A)
Reference Rs561367199(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ASL
CLNDBN not specified not provided
Reversed 0
HGVS NC_000007.13:g.65547907G>A
CLNSRC
CLNACC RCV000272723.1, RCV000493464.1,