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rs1064795835

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position7445128
GeneCHRNB1, FGF11
is asnp
is mentioned by
dbSNPrs1064795835
dbSNP (old)rs1064795835
ClinGenrs1064795835
ebirs1064795835
HLIrs1064795835
Exacrs1064795835
Gnomadrs1064795835
Varsomers1064795835
Maprs1064795835
PheGenIrs1064795835
Biobankrs1064795835
1000 genomesrs1064795835
hgdprs1064795835
ensemblrs1064795835
gopubmedrs1064795835
geneviewrs1064795835
scholarrs1064795835
googlers1064795835
pharmgkbrs1064795835
gwascentralrs1064795835
openSNPrs1064795835
23andMers1064795835
23andMe allrs1064795835
SNPshotrs1064795835
SNPdbers1064795835
MSV3drs1064795835
GWAS Ctlgrs1064795835
Max Magnitude0
ClinVar
Risk rs1064795835(G;G)
Alt rs1064795835(G;G)
Reference Rs1064795835(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHRNB1 FGF11
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7348447A>G
CLNSRC
CLNACC RCV000482140.1,