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rs863224028

From SNPedia

Orientationplus
Make rs863224028(-;-)
Make rs863224028(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position1984417
GeneGFER
is asnp
is mentioned by
dbSNPrs863224028
ebirs863224028
HLIrs863224028
Exacrs863224028
Varsomers863224028
Maprs863224028
PheGenIrs863224028
hapmaprs863224028
1000 genomesrs863224028
hgdprs863224028
ensemblrs863224028
gopubmedrs863224028
geneviewrs863224028
scholarrs863224028
googlers863224028
pharmgkbrs863224028
gwascentralrs863224028
openSNPrs863224028
23andMers863224028
23andMe allrs863224028
SNP Nexus

SNPshotrs863224028
SNPdbers863224028
MSV3drs863224028
GWAS Ctlgrs863224028
Max Magnitude
ClinVar
Risk rs863224028(;)
Alt rs863224028(;)
Reference rs863224028(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFER
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2034418delC
CLNSRC
CLNACC RCV000200750.1,