Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/C | MAF: 0.34 (-)
Location

Chromosome 7: between 100316548 and 100316549 (forward strand) | View in location tab

Most severe consequence
HGVS name

7:g.100316548_100316549insC

Variation displays