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rs1057517204

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517204(A;A)
Make rs1057517204(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position186285637
GeneF11, F11-AS1
is asnp
is mentioned by
dbSNPrs1057517204
dbSNP (old)rs1057517204
ClinGenrs1057517204
ebirs1057517204
HLIrs1057517204
Exacrs1057517204
Gnomadrs1057517204
Varsomers1057517204
Maprs1057517204
PheGenIrs1057517204
Biobankrs1057517204
1000 genomesrs1057517204
hgdprs1057517204
ensemblrs1057517204
gopubmedrs1057517204
geneviewrs1057517204
scholarrs1057517204
googlers1057517204
pharmgkbrs1057517204
gwascentralrs1057517204
openSNPrs1057517204
23andMers1057517204
23andMe allrs1057517204
SNPshotrs1057517204
SNPdbers1057517204
MSV3drs1057517204
GWAS Ctlgrs1057517204
Max Magnitude0
ClinVar
Risk rs1057517204(A;A)
Alt rs1057517204(A;A)
Reference Rs1057517204(G;G)
Significance Probable-Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11-AS1 F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187206791G>A
CLNSRC
CLNACC RCV000410824.1,