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

rs756998699

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756998699(A;A)
Make rs756998699(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position48898785
GeneSLC25A20
is asnp
is mentioned by
dbSNPrs756998699
ebirs756998699
HLIrs756998699
Exacrs756998699
Varsomers756998699
Maprs756998699
PheGenIrs756998699
hapmaprs756998699
1000 genomesrs756998699
hgdprs756998699
ensemblrs756998699
gopubmedrs756998699
geneviewrs756998699
scholarrs756998699
googlers756998699
pharmgkbrs756998699
gwascentralrs756998699
openSNPrs756998699
23andMers756998699
23andMe allrs756998699
SNP Nexus

SNPshotrs756998699
SNPdbers756998699
MSV3drs756998699
GWAS Ctlgrs756998699
Max Magnitude0
ClinVar
Risk rs756998699(A;A) rs756998699(C;C)
Alt rs756998699(A;A) rs756998699(C;C)
Reference Rs756998699(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC25A20
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.48936218G>A
CLNSRC
CLNACC RCV000186165.2,