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

rs145297855

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145297855(C;T)
Make rs145297855(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position87529647
GeneRARS2
is asnp
is mentioned by
dbSNPrs145297855
ebirs145297855
HLIrs145297855
Exacrs145297855
Varsomers145297855
Maprs145297855
PheGenIrs145297855
hapmaprs145297855
1000 genomesrs145297855
hgdprs145297855
ensemblrs145297855
gopubmedrs145297855
geneviewrs145297855
scholarrs145297855
googlers145297855
pharmgkbrs145297855
gwascentralrs145297855
openSNPrs145297855
23andMers145297855
23andMe allrs145297855
SNP Nexus

SNPshotrs145297855
SNPdbers145297855
MSV3drs145297855
GWAS Ctlgrs145297855
Max Magnitude0
ClinVar
Risk rs145297855(A,T;A,T)
Alt rs145297855(A,T;A,T)
Reference rs145297855(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.88239365C>T
CLNSRC
CLNACC RCV000198712.1,