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

rs757649757

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757649757(A;G)
Make rs757649757(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position197705550
GeneMARS2
is asnp
is mentioned by
dbSNPrs757649757
ebirs757649757
HLIrs757649757
Exacrs757649757
Varsomers757649757
Maprs757649757
PheGenIrs757649757
hapmaprs757649757
1000 genomesrs757649757
hgdprs757649757
ensemblrs757649757
gopubmedrs757649757
geneviewrs757649757
scholarrs757649757
googlers757649757
pharmgkbrs757649757
gwascentralrs757649757
openSNPrs757649757
23andMers757649757
23andMe allrs757649757
SNP Nexus

SNPshotrs757649757
SNPdbers757649757
MSV3drs757649757
GWAS Ctlgrs757649757
Max Magnitude0
ClinVar
Risk rs757649757(G;G)
Alt rs757649757(G;G)
Reference rs757649757(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MARS2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.198570274A>G
CLNSRC
CLNACC RCV000195832.1,