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rs147568500

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147568500(A;A)
Make rs147568500(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position1986002
GeneGFER
is asnp
is mentioned by
dbSNPrs147568500
ebirs147568500
HLIrs147568500
Exacrs147568500
Varsomers147568500
Maprs147568500
PheGenIrs147568500
hapmaprs147568500
1000 genomesrs147568500
hgdprs147568500
ensemblrs147568500
gopubmedrs147568500
geneviewrs147568500
scholarrs147568500
googlers147568500
pharmgkbrs147568500
gwascentralrs147568500
openSNPrs147568500
23andMers147568500
23andMe allrs147568500
SNP Nexus

SNPshotrs147568500
SNPdbers147568500
MSV3drs147568500
GWAS Ctlgrs147568500
Max Magnitude0
ClinVar
Risk rs147568500(A;A)
Alt rs147568500(A;A)
Reference rs147568500(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFER
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2036003G>A
CLNSRC
CLNACC RCV000196297.1,