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Variant (rsID / SNP)

rs816736

GEMIN5

rs816736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GEMIN5. Location: chromosome 5, position 154,271,948. The table records no clinical significance for this variant.

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Reference-table entries

GEMIN5Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
5:154271948
HGVS
NM_015465.5,c.3759C>T,p.Asp1253Asp
Allele change
Synonymous_D1253D

Public references

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