Variant (rsID / SNP)

rs149562038

rs149562038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCF2. Clinical significance in the table: Likely benign.

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Reference-table entries

MCF2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xq27.1
HGVS: NM_001171876.2(MCF2):c.2008A>G (p.Asn670Asp)
Allele change: Missense_N594D

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.