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rs727505371

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs727505371(-;-)
Make rs727505371(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position38421840
GeneFGFR1
is asnp
is mentioned by
dbSNPrs727505371
ebirs727505371
HLIrs727505371
Exacrs727505371
Varsomers727505371
Maprs727505371
PheGenIrs727505371
hapmaprs727505371
1000 genomesrs727505371
hgdprs727505371
ensemblrs727505371
gopubmedrs727505371
geneviewrs727505371
scholarrs727505371
googlers727505371
pharmgkbrs727505371
gwascentralrs727505371
openSNPrs727505371
23andMers727505371
23andMe allrs727505371
SNP Nexus

SNPshotrs727505371
SNPdbers727505371
MSV3drs727505371
GWAS Ctlgrs727505371
Max Magnitude0
ClinVar
Risk rs727505371(;)
Alt rs727505371(;)
Reference rs727505371(CT;CT)
Significance Probable-Pathogenic
Disease Hypogonadotrophic hypogonadism Delayed puberty
Variation info
Gene FGFR1
CLNDBN Hypogonadotrophic hypogonadism Delayed puberty
Reversed 1
HGVS NC_000008.10:g.38279358_38279359delAG
CLNSRC
CLNACC RCV000156957.1, RCV000156958.1,