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rs1057520762

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520762(A;A)
Make rs1057520762(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position67744677
GeneGNRHR
is asnp
is mentioned by
dbSNPrs1057520762
dbSNP (old)rs1057520762
ClinGenrs1057520762
ebirs1057520762
HLIrs1057520762
Exacrs1057520762
Gnomadrs1057520762
Varsomers1057520762
LitVarrs1057520762
Maprs1057520762
PheGenIrs1057520762
Biobankrs1057520762
1000 genomesrs1057520762
hgdprs1057520762
ensemblrs1057520762
gopubmedrs1057520762
geneviewrs1057520762
scholarrs1057520762
googlers1057520762
pharmgkbrs1057520762
gwascentralrs1057520762
openSNPrs1057520762
23andMers1057520762
23andMe allrs1057520762
SNPshotrs1057520762
SNPdbers1057520762
MSV3drs1057520762
GWAS Ctlgrs1057520762
Max Magnitude0
ClinVar
Risk rs1057520762(A;A)
Alt rs1057520762(A;A)
Reference Rs1057520762(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GNRHR
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.68610395A>T
CLNSRC
CLNACC RCV000418487.1,