Have questions? Visit https://www.reddit.com/r/SNPedia

rs201007090

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201007090(A;A)
Make rs201007090(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position186286490
GeneF11, F11-AS1
is asnp
is mentioned by
dbSNPrs201007090
ebirs201007090
HLIrs201007090
Exacrs201007090
Varsomers201007090
Maprs201007090
PheGenIrs201007090
hapmaprs201007090
1000 genomesrs201007090
hgdprs201007090
ensemblrs201007090
gopubmedrs201007090
geneviewrs201007090
scholarrs201007090
googlers201007090
pharmgkbrs201007090
gwascentralrs201007090
openSNPrs201007090
23andMers201007090
23andMe allrs201007090
SNP Nexus

SNPshotrs201007090
SNPdbers201007090
MSV3drs201007090
GWAS Ctlgrs201007090
Max Magnitude0
ClinVar
Risk rs201007090(A;A)
Alt rs201007090(A;A)
Reference rs201007090(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.187207644G>A
CLNSRC
CLNACC RCV000169241.1,