Variant (rsID / SNP)

rs6587625

rs6587625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THEM5. Location: chromosome 1, position 151,820,324. The table records no clinical significance for this variant.

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Reference-table entries

THEM5Not classified

Variant type: missense_variant
Chromosome / position: 1:151820324
HGVS: NM_182578.4,c.590A>G,p.Asp197Gly
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.