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rs6108011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6108011(C;T)
Make rs6108011(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position7571857
is asnp
is mentioned by
dbSNPrs6108011
ebirs6108011
HLIrs6108011
Exacrs6108011
Varsomers6108011
Maprs6108011
PheGenIrs6108011
hapmaprs6108011
1000 genomesrs6108011
hgdprs6108011
ensemblrs6108011
gopubmedrs6108011
geneviewrs6108011
scholarrs6108011
googlers6108011
pharmgkbrs6108011
gwascentralrs6108011
openSNPrs6108011
23andMers6108011
23andMe allrs6108011
SNP Nexus

SNPshotrs6108011
SNPdbers6108011
MSV3drs6108011
GWAS Ctlgrs6108011
GMAF0.2594
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


[PMID 17186469OA-icon.png] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.


GET Evidence
rs6108011
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary