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rs7 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:92150243 (GRCh38)
7:91779557 (GRCh37)
Canonical SPDI:: NC_000007.14:92150242:T:A
Gene:: LRRD1 (Varview), CYP51A1-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00757/143 (ALFA)
A=0.004367/1156 (TOPMED)
A=0.00501/5 (GoNL)
A=0.005394/20 (TWINSUK)
A=0.006393/954 (GnomAD_genomes)
A=0.006667/4 (NorthernSweden)
A=0.006746/26 (ALSPAC)
A=0.007495/48 (1000Genomes_30X)
A=0.007788/39 (1000Genomes)
A=0.015179/68 (Estonian)
A=0.032407/7 (Qatari)
T=0.5/1 (Siberian)
T=0.5/3 (SGDP_PRJ)
HGVS:: NC_000007.14:g.92150243T>A, NC_000007.13:g.91779557T>A

dbSNP