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rs727505376

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505376(A;A)
Make rs727505376(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position38414279
GeneFGFR1
is asnp
is mentioned by
dbSNPrs727505376
ebirs727505376
HLIrs727505376
Exacrs727505376
Varsomers727505376
Maprs727505376
PheGenIrs727505376
hapmaprs727505376
1000 genomesrs727505376
hgdprs727505376
ensemblrs727505376
gopubmedrs727505376
geneviewrs727505376
scholarrs727505376
googlers727505376
pharmgkbrs727505376
gwascentralrs727505376
openSNPrs727505376
23andMers727505376
23andMe allrs727505376
SNP Nexus

SNPshotrs727505376
SNPdbers727505376
MSV3drs727505376
GWAS Ctlgrs727505376
Max Magnitude0
ClinVar
Risk rs727505376(A;A)
Alt rs727505376(A;A)
Reference rs727505376(G;G)
Significance Probable-Pathogenic
Disease Hypogonadotrophic hypogonadism
Variation info
Gene FGFR1
CLNDBN Hypogonadotrophic hypogonadism
Reversed 1
HGVS NC_000008.10:g.38271797C>T
CLNSRC
CLNACC RCV000156967.1,