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rs1057520036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520036(A;G)
Make rs1057520036(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177093180
GeneFGFR4
is asnp
is mentioned by
dbSNPrs1057520036
dbSNP (classic)rs1057520036
ClinGenrs1057520036
ebirs1057520036
HLIrs1057520036
Exacrs1057520036
Gnomadrs1057520036
Varsomers1057520036
LitVarrs1057520036
Maprs1057520036
PheGenIrs1057520036
Biobankrs1057520036
1000 genomesrs1057520036
hgdprs1057520036
ensemblrs1057520036
geneviewrs1057520036
scholarrs1057520036
googlers1057520036
pharmgkbrs1057520036
gwascentralrs1057520036
openSNPrs1057520036
23andMers1057520036
23andMe allrs1057520036
SNPshotrs1057520036
SNPdbers1057520036
MSV3drs1057520036
GWAS Ctlgrs1057520036
Max Magnitude0
ClinVar
Risk rs1057520036(G;G)
Alt rs1057520036(G;G)
Reference Rs1057520036(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of breast
Variation info
Gene FGFR4
CLNDBN Neoplasm of breast
Reversed 0
HGVS NC_000005.9:g.176520181A>G
CLNSRC
CLNACC RCV000433453.1,