Variant (rsID / SNP)

rs1592624

rs1592624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSMD3. Location: chromosome 8, position 113,241,088. The table records no clinical significance for this variant.

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Reference-table entries

CSMD3Not classified

Variant type: missense_variant
Chromosome / position: 8:113241088
HGVS: NM_198123.2,c.10861A>C,p.Asn3621His
Allele change: Missense_N3421H

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.