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rs672601339

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601339(G;T)
Make rs672601339(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position1270787
GeneBHLHA9
is asnp
is mentioned by
dbSNPrs672601339
ebirs672601339
HLIrs672601339
Exacrs672601339
Varsomers672601339
Maprs672601339
PheGenIrs672601339
hapmaprs672601339
1000 genomesrs672601339
hgdprs672601339
ensemblrs672601339
gopubmedrs672601339
geneviewrs672601339
scholarrs672601339
googlers672601339
pharmgkbrs672601339
gwascentralrs672601339
openSNPrs672601339
23andMers672601339
23andMe allrs672601339
SNP Nexus

SNPshotrs672601339
SNPdbers672601339
MSV3drs672601339
GWAS Ctlgrs672601339
Max Magnitude0
ClinVar
Risk rs672601339(T;T)
Alt rs672601339(T;T)
Reference rs672601339(G;G)
Significance Pathogenic
Disease Syndactyly type 9
Variation info
Gene BHLHA9
CLNDBN Syndactyly type 9
Reversed 0
HGVS NC_000017.10:g.1174081G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149488.5,