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rs1057520549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520549(C;T)
Make rs1057520549(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position147639258
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1057520549
dbSNP (old)rs1057520549
ClinGenrs1057520549
ebirs1057520549
HLIrs1057520549
Exacrs1057520549
Gnomadrs1057520549
Varsomers1057520549
LitVarrs1057520549
Maprs1057520549
PheGenIrs1057520549
Biobankrs1057520549
1000 genomesrs1057520549
hgdprs1057520549
ensemblrs1057520549
gopubmedrs1057520549
geneviewrs1057520549
scholarrs1057520549
googlers1057520549
pharmgkbrs1057520549
gwascentralrs1057520549
openSNPrs1057520549
23andMers1057520549
23andMe allrs1057520549
SNPshotrs1057520549
SNPdbers1057520549
MSV3drs1057520549
GWAS Ctlgrs1057520549
Max Magnitude0
ClinVar
Risk rs1057520549(T;T)
Alt rs1057520549(T;T)
Reference Rs1057520549(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.147336350C>T
CLNSRC
CLNACC RCV000423733.1,