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rs864309719

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309719(A;G)
Make rs864309719(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position35070275
GeneMAPRE2
is asnp
is mentioned by
dbSNPrs864309719
ebirs864309719
HLIrs864309719
Exacrs864309719
Varsomers864309719
Maprs864309719
PheGenIrs864309719
hapmaprs864309719
1000 genomesrs864309719
hgdprs864309719
ensemblrs864309719
gopubmedrs864309719
geneviewrs864309719
scholarrs864309719
googlers864309719
pharmgkbrs864309719
gwascentralrs864309719
openSNPrs864309719
23andMers864309719
23andMe allrs864309719
SNP Nexus

SNPshotrs864309719
SNPdbers864309719
MSV3drs864309719
GWAS Ctlgrs864309719
Max Magnitude0
ClinVar
Risk rs864309719(G;G)
Alt rs864309719(G;G)
Reference rs864309719(A;A)
Significance Pathogenic
Disease Skin creases
Variation info
Gene MAPRE2
CLNDBN Skin creases, congenital symmetric circumferential, 2
Reversed 0
HGVS NC_000018.9:g.32650239A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000203276.1,