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rs771809901

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771809901(C;T)
Make rs771809901(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position1984861
GeneGFER
is asnp
is mentioned by
dbSNPrs771809901
ebirs771809901
HLIrs771809901
Exacrs771809901
Varsomers771809901
Maprs771809901
PheGenIrs771809901
hapmaprs771809901
1000 genomesrs771809901
hgdprs771809901
ensemblrs771809901
gopubmedrs771809901
geneviewrs771809901
scholarrs771809901
googlers771809901
pharmgkbrs771809901
gwascentralrs771809901
openSNPrs771809901
23andMers771809901
23andMe allrs771809901
SNP Nexus

SNPshotrs771809901
SNPdbers771809901
MSV3drs771809901
GWAS Ctlgrs771809901
Max Magnitude0
ClinVar
Risk rs771809901(T;T)
Alt rs771809901(T;T)
Reference rs771809901(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GFER
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2034862C>T
CLNSRC
CLNACC RCV000199819.1,