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

rs797045249

From SNPedia

Orientationplus
Make rs797045249(-;-)
Make rs797045249(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position100101746
GeneAP4M1, MCM7
is asnp
is mentioned by
dbSNPrs797045249
ebirs797045249
HLIrs797045249
Exacrs797045249
Varsomers797045249
Maprs797045249
PheGenIrs797045249
hapmaprs797045249
1000 genomesrs797045249
hgdprs797045249
ensemblrs797045249
gopubmedrs797045249
geneviewrs797045249
scholarrs797045249
googlers797045249
pharmgkbrs797045249
gwascentralrs797045249
openSNPrs797045249
23andMers797045249
23andMe allrs797045249
SNP Nexus

SNPshotrs797045249
SNPdbers797045249
MSV3drs797045249
GWAS Ctlgrs797045249
Max Magnitude
ClinVar
Risk rs797045249(;)
Alt rs797045249(;)
Reference rs797045249(A;A)
Significance Probable-Pathogenic
Disease Spastic paraplegia 50
Variation info
Gene MCM7 AP4M1
CLNDBN Spastic paraplegia 50, autosomal recessive
Reversed 0
HGVS NC_000007.13:g.99699369delA
CLNSRC
CLNACC RCV000193994.1,