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

rs549522925

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs549522925(A;A)
Make rs549522925(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position149582208
GeneMMADHC
is asnp
is mentioned by
dbSNPrs549522925
ebirs549522925
HLIrs549522925
Exacrs549522925
Varsomers549522925
Maprs549522925
PheGenIrs549522925
hapmaprs549522925
1000 genomesrs549522925
hgdprs549522925
ensemblrs549522925
gopubmedrs549522925
geneviewrs549522925
scholarrs549522925
googlers549522925
pharmgkbrs549522925
gwascentralrs549522925
openSNPrs549522925
23andMers549522925
23andMe allrs549522925
SNP Nexus

SNPshotrs549522925
SNPdbers549522925
MSV3drs549522925
GWAS Ctlgrs549522925
Max Magnitude0
ClinVar
Risk rs549522925(A,G;A,G)
Alt rs549522925(A,G;A,G)
Reference rs549522925(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MMADHC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.150438722C>A
CLNSRC
CLNACC RCV000186038.1,