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rs727505377

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505377(C;C)
Make rs727505377(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position38414001
GeneFGFR1
is asnp
is mentioned by
dbSNPrs727505377
ebirs727505377
HLIrs727505377
Exacrs727505377
Varsomers727505377
Maprs727505377
PheGenIrs727505377
hapmaprs727505377
1000 genomesrs727505377
hgdprs727505377
ensemblrs727505377
gopubmedrs727505377
geneviewrs727505377
scholarrs727505377
googlers727505377
pharmgkbrs727505377
gwascentralrs727505377
openSNPrs727505377
23andMers727505377
23andMe allrs727505377
SNP Nexus

SNPshotrs727505377
SNPdbers727505377
MSV3drs727505377
GWAS Ctlgrs727505377
Max Magnitude0
ClinVar
Risk rs727505377(C;C)
Alt rs727505377(C;C)
Reference rs727505377(T;T)
Significance Probable-Pathogenic
Disease Hypogonadotrophic hypogonadism
Variation info
Gene FGFR1
CLNDBN Hypogonadotrophic hypogonadism
Reversed 1
HGVS NC_000008.10:g.38271519A>G
CLNSRC
CLNACC RCV000156969.1,