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rs104893956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893956(C;T)
Make rs104893956(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position151842613
GeneESR1
is asnp
is mentioned by
dbSNPrs104893956
ebirs104893956
HLIrs104893956
Exacrs104893956
Varsomers104893956
Maprs104893956
PheGenIrs104893956
hapmaprs104893956
1000 genomesrs104893956
hgdprs104893956
ensemblrs104893956
gopubmedrs104893956
geneviewrs104893956
scholarrs104893956
googlers104893956
pharmgkbrs104893956
gwascentralrs104893956
openSNPrs104893956
23andMers104893956
23andMe allrs104893956
SNP Nexus

SNPshotrs104893956
SNPdbers104893956
MSV3drs104893956
GWAS Ctlgrs104893956
Max Magnitude0
OMIM133430
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893956(T;T)
Alt rs104893956(T;T)
Reference rs104893956(C;C)
Significance Pathogenic
Disease Estrogen resistance
Variation info
Gene ESR1
CLNDBN Estrogen resistance
Reversed 0
HGVS NC_000006.11:g.152163748C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018060.29,