Variant (rsID / SNP)

rs61738268

rs61738268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERMARD. Location: chromosome 6, position 170,169,688. Clinical significance in the table: Benign.

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Reference-table entries

ERMARDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:170169688
Cytoband: 6q27
HGVS: NM_018341.3(ERMARD):c.1112A>G (p.His371Arg)
Allele change: Missense_H371R

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.