Variant (rsID / SNP)

rs6001930

rs6001930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRTFA. Location: chromosome 22, position 40,876,234. Clinical significance in the table: Benign.

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Reference-table entries

MRTFABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:40876234
Cytoband: 22q13.1
HGVS: NM_020831.6(MRTFA):c.242-16944A>G
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.