Variant (rsID / SNP)

rs7178698

rs7178698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCTP2. Location: chromosome 15, position 94,945,719. The table records no clinical significance for this variant.

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Reference-table entries

MCTP2Not classified

Variant type: missense_variant
Chromosome / position: 15:94945719
HGVS: NM_001385008.1,c.2090G>T,p.Arg697Leu
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.