Variant (rsID / SNP)

rs11844594

rs11844594 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SAMD15. Location: chromosome 14, position 77,843,814. The table records no clinical significance for this variant.

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Reference-table entries

SAMD15Not classified

Variant type: missense_variant
Chromosome / position: 14:77843814
HGVS: NM_001010860.4,c.53T>C,p.Leu18Pro
Allele change: Missense_L18P

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.