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rs267606621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606621(A;A)
Make rs267606621(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position70268356
GeneAARS
is asnp
is mentioned by
dbSNPrs267606621
ebirs267606621
HLIrs267606621
Exacrs267606621
Varsomers267606621
Maprs267606621
PheGenIrs267606621
hapmaprs267606621
1000 genomesrs267606621
hgdprs267606621
ensemblrs267606621
gopubmedrs267606621
geneviewrs267606621
scholarrs267606621
googlers267606621
pharmgkbrs267606621
gwascentralrs267606621
openSNPrs267606621
23andMers267606621
23andMe allrs267606621
SNP Nexus

SNPshotrs267606621
SNPdbers267606621
MSV3drs267606621
GWAS Ctlgrs267606621
Max Magnitude0
ClinVar
Risk rs267606621(A;A)
Alt rs267606621(A;A)
Reference rs267606621(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease
Variation info
Gene AARS
CLNDBN Charcot-Marie-Tooth disease, type 2N Charcot-Marie-Tooth disease, type 2 Charcot-Marie-Tooth disease
Reversed 1
HGVS NC_000016.9:g.70302259C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008987.3, RCV000168406.1, RCV000192253.1,